EXTENDED RELEASE COMPOSITIONS OF PSEUDOEPHEDRINE OR ITS PHARMACEUTICALLY ACCEPTABLE SALT THEREOF

Abstract

This invention relates to dosage forms comprising pseudoephedrine or a salt thereof, for extended-release up to 24 hours, and process of making such dosage forms. This invention provides a non-osmotic extended-release dosage form comprising pseudoephedrine hydrochloride which can be administered to patients who need and/or desire a decongestant medication up to 24 hours. This invention also relates to dosage forms comprising pseudoephedrine or a salt thereof and cetirizine or levocetirizine or its salts thereof for extended-release up to 24 hours, and process of making such dosage forms.

Claims

1. A non-osmotic extended release formulation comprising pseudoephedrine or a salt thereof, comprising: I. a core comprising: a) about 60% to 90% of pseudoephedrine or a salt thereof by total weight of pseudoephedrine or a salt thereof; b) a water soluble extended release polymer; and c) one or more other pharmaceutical excipients; II. optional seal coat; III. extended-release coating comprising: cellulose acetate, at least one plasticizer, at least one pore-former; IV. optional sub coat; and V. an immediate release coating comprising about 10% to 40% of pseudoephedrine or a salt thereof by total weight of pseudoephedrine or a salt thereof, and one or more other pharmaceutical excipients.

2. The extended release formulation of claim 1, wherein the amount of pseudoephedrine hydrochloride is present in core is about 75% and wherein the amount of pseudoephedrine hydrochloride is present in immediate release coating is about 25%.

3. The extended release formulation of claim 1, wherein the amount of pseudoephedrine hydrochloride is present in core is about 180 mg, the water soluble extended release polymer is present in an amount of about 40% to 60% of by total weight of the core tablet and the said polymer is hydroxypropylmethyl cellulose, and the amount of pseudoephedrine hydrochloride is present in immediate release coating is about 60 mg.

4. The extended release formulation of claim 1, wherein the weight ratio of cellulose acetate, plasticizer and pore former in the extended release coating is from about 1:0.1:0.1 to 1:1.5:1.5.

5. The extended release formulation of claim 1, wherein plasticizer is selected from the group comprising of dibutyl sebacate, triacetin, diethyl phthalate, tributyl sebacate, glycerin, triacetin, and triethyl citrate or mixtures thereof.

6. The extended release formulation of claim 5, wherein the plasticizer is dibutyl sebacate.

7. The extended release formulation of claim 1, wherein pore-former is selected from the group comprising of polyethylene glycol, hydroxypropylmethyl cellulose, hydroxypropyl cellulose, glucose, fructose, mannitol, sorbitol, dextran, polyvinylpyrrolidone, polypropylene glycol or mixtures thereof.

8. The extended release formulation of claim 7, wherein the pore-former is polyethylene glycol.

9. A non-osmotic extended release tablet comprising: I. a core comprising: a) about 180 mg of pseudoephedrine hydrochloride; b) hydroxypropylmethyl cellulose; and c) one or more other pharmaceutical excipients; II. optional seal coat; III. extended release coating comprising: about 50% to 75% weight of cellulose acetate, and about 25% to 50% weight mixture of dibutyl sebecate and polyethylene glycol, by total weight of extended release coating composition, wherein the weight ratio of cellulose acetate, dibutyl sebecate and polyethylene glycol is from about 1:0.1:0.1 to 1:0.3:0.5; IV. optional sub coat; and V. an immediate release coating comprising about 60 mg of pseudoephedrine hydrochloride and hydroxypropylmethyl cellulose.

10. The extended release tablet of claim 9, wherein the amount of hydroxypropylmethyl cellulose is present in core is about 40% to 60% of by total weight of the core tablet.

11. The extended release tablet of claim 9, wherein the weight ratio of cellulose acetate, dibutyl sebecate and polyethylene glycol in the extended release coating is 1:0.15:0.3.

12. The extended release tablet of claim 9, wherein the core tablet is prepared by direct compression process.

13. The amount of drug released from the extended release tablet of claim 9, is from about 20% to 35% at 2 hours, from about 40% to 75% at 8 hours, from about 65% to 90% at 12 hours and not less than 85% at 24 hours.

14. The extended release formulation of claim 1, is used for the relief of symptoms associated with nasal congestion in adults and children 12 years of age and older.

15. The non-osmotic extended release tablet composition of claim 9, further comprising cetirizine or levocetirizine or its salt thereof in the immediate release coating.

Description

DETAILED DESCRIPTION OF THE INVENTION

[0039] The present invention relates to non-osmotic extended-release pharmaceutical formulations comprising pseudoephedrine or its pharmaceutical salts, having an immediate release phase, followed by drug delivery at a controlled rate over a period of time, preferably up to 24 hours.

[0040] As used herein, the term “pseudoephedrine” includes the compound pseudoephedrine and any of its pharmaceutically acceptable salts, polymorphs, solvates, esters, hydrates, enantiomers, racemates, and mixtures thereof. Preferably, it is pseudoephedrine hydrochloride.

[0041] As used herein, the term “controlled release (CR)” or “extended release (ER)” indicates a formulation that releases drug in a manner different from that of an immediate release dosage form (in which drug release commences promptly in the stomach after oral administration, and continues at a rapid rate as the dosage form disintegrates), such as providing a drug release that is delayed for a desired time period after administration, and/or a drug release that occurs during a desired time period after administration. The terms ‘sustained’, ‘extended’, ‘delayed’, ‘modified’, or ‘prolonged’ are included within the term “controlled,” and as applied include any drug delivery system which achieves the release of drug after and/or over a desired period of time, e.g., providing dosage forms that can be administered every 8 hours, 12 hours, 24 hours, etc. The drug delivery systems include those such as modified-release matrix cores, modified-release matrix cores coated with a release-modifying coating, enteric coated dosage forms, dosage forms surrounded by a release-modifying coating, gastro-retentive dosage forms, muco-adhesive dosage forms, osmotic release dosage forms, etc. Immediate release (IR) pseudoephedrine products typically require dosing at 4-6 hour intervals, to provide the desired therapeutic effect.

[0042] The terms “dosage form” or “composition” or “formulation” as used herein relate to solid orally administered units comprising a drug and one or more pharmacologically inert excipients, such as tablets, mini-tablets, caplets, capsules, granules, pills, powders, microparticles, nanoparticles, etc.

[0043] The term “functional coating” relates to any type of coating that modifies the release of pseudoephedrine or its salts from a dosage form. The rate-controlling polymers or extended release polymers or its combinations with have a significant role in modification of the release of pseudoephedrine or its salts from a dosage form.

[0044] To provide a more concise description, some of the quantitative expressions given herein are not qualified with the term “about”. It is understood that whether the term “about” is used explicitly or not, every quantity given herein is meant to refer to the actual given value, and it is also meant to refer to the approximation to such given value that would reasonably be inferred based on the ordinary skill in the art, including approximations due to the experimental and/or measurement conditions for such given value.

[0045] The term “core” as used herein is defined to mean a particle or a solid vehicle, into which, or onto which, pseudoephedrine is uniformly or non-uniformly dispersed. A drug-containing core will desirably be formed by methods and materials well known in the art, such as for example by compressing, fusing, or extruding pseudoephedrine alone or together with at least one pharmaceutically acceptable excipient, or coating a pseudoephedrine composition onto a pharmacologically inert substrate.

[0046] In an embodiment, the present invention provides a non-osmotic extended release formulation comprising pseudoephedrine or a salt thereof, comprising:

[0047] I. a core comprising: a) about 60% to 90% of pseudoephedrine or a salt thereof by total weight of pseudoephedrine or a salt thereof; b) a water soluble extended release polymer; and c) one or more other pharmaceutical excipients;

[0048] II. optional seal coat;

[0049] III. extended-release coating comprising: cellulose acetate, at least one plasticizer, at least one pore-former;

[0050] IV. optional sub coat; and

[0051] V. an immediate release coating comprising about 10% to 40% of pseudoephedrine or a salt thereof by total weight of pseudoephedrine or a salt thereof, and one or more other pharmaceutical excipients.

[0052] For example core is a compressed tablet comprising about 180 mg of pseudoephedrine hydrochloride, hydroxypropylmethyl cellulose, and one or more other pharmaceutical excipients selected from diluents, binders, glidants, lubricants and others.

[0053] Exemplary diluents include, but not limited to, lactose, microcrystalline cellulose, sucrose, mannitol, xylitol, erythritol, sorbitol, maltitol, calcium citrate, calcium phosphate, and calcium aluminometasilicate, calcium carbonate, calcium phosphate, dicalcium phosphate, calcium sulfate, dextrin/dextrates, maltodextrin, and compressible sugars or mixtures thereof.

[0054] Exemplary lubricants include magnesium stearate, zinc stearate, calcium stearate, talc, carnauba wax, stearic acid, palmitic acid, sodium stearyl fumarate, sodium lauryl sulfate, glyceryl palmitostearate, palmitic acid, myristic acid and hydrogenated vegetable oils and fats.

[0055] Exemplary glidants include talc, colloidal silicon dioxide, silicic acid, calcium silicate, magnesium carbonate, magnesium oxide, magnesium silicate, starch, castor wax and the like.

[0056] Preferably, core tablet is a compressed tablet comprising about 180 mg of pseudoephedrine hydrochloride, hydroxypropylmethyl cellulose, lactose monohydrate, microcrystalline cellulose, colloidal silicon dioxide, stearic acid. The process of making such compressed tablet can be according to standard techniques of tableting viz; direct compression or wet granulation or dry granulation. The direct compression is being preferred.

[0057] Exemplary water soluble extended release polymers include, but are not limited to, hydroxypropyl methyl cellulose (HPMC), sodium alginate, hydroxypropyl cellulose, methyl cellulose, carboxymethyl cellulose, or mixtures thereof. Preferred water soluble extended release polymer is hydroxypropyl methyl cellulose.

[0058] Exemplary plasticizers, include but are not limited to, dibutyl sebacate, triacetin, diethyl phthalate, tributyl sebacate, glycerin, triacetin, and triethyl citrate or mixtures thereof.

[0059] Exemplary pore formers, include but are not limited to, polyethylene glycols, hydroxypropylmethyl cellulose, hydroxypropyl cellulose, glucose, fructose, mannitol, sorbitol, dextran, polyvinylpyrrolidone, polypropylene glycols or mixtures thereof.

[0060] Seal coat or sub coat can be formed by conventional coating techniques with various useful film-forming agents include, but are not limited to, cellulose or its derivatives including soluble alkyl- or hydroalkyl-cellulose derivatives such as methylcelluloses, hydroxymethyl celluloses, hydroxyethyl celluloses, hydroxypropyl celluloses, hydroxymethyethyl celluloses, hydroxypropyl methylcelluloses, sodium carboxymethyl celluloses, etc., acidic cellulose derivatives such as cellulose acetate phthalates, cellulose acetate trimellitates, and methylhydroxypropylcellulose phthalates, polyvinylacetate phthalates, etc., insoluble cellulose derivatives such as ethylcelluloses and the like, dextrins, starches and starch derivatives, polymers based on carbohydrates and derivatives thereof, natural gums such as gum Arabic, xanthans, alginates, poly acrylic acids, polyvinylalcohols, polyvinylacetates, polyvinylpyrrolidones, polymethacrylates and derivatives thereof (Eudragit.™.), chitosan and derivatives thereof, shellac and derivatives thereof, and waxes and fat substances. Instant coating materials that are commercially available in the market also can be used such as OPADRY coating materials including Opadry AMB II 88A180040 white which contains polyvinyl alcohol, talc, titanium dioxide, glycerylmonocaprylocaprate, sodium lauryl sulfate.

[0061] In an embodiment, the present invention provides a non-osmotic extended release tablet comprising pseudoephedrine hydrochloride, comprising:

[0062] I. a tablet core comprising: a) about 60% to 90% of pseudoephedrine hydrochloride by total weight of pseudoephedrine hydrochloride; b) hydroxypropylmethyl cellulose; and c) one or more other pharmaceutical excipients;

[0063] II. optional seal coat;

[0064] III. extended release coating comprising: cellulose acetate, dibutyl sebacate, polyethylene glycol;

[0065] IV. optional sub coat; and

[0066] V. an immediate release coating comprising about 10% to 40% of pseudoephedrine hydrochloride by total weight of pseudoephedrine hydrochloride, and one or more other pharmaceutical excipients.

[0067] In an embodiment, the present invention provides a non-osmotic extended release tablet comprising pseudoephedrine hydrochloride, comprising:

[0068] I. a tablet core comprising: a) about 60% to 90% of pseudoephedrine hydrochloride by total weight of pseudoephedrine hydrochloride; about 40% to 60% of hydroxypropylmethyl cellulose; and c) one or more other pharmaceutical excipients;

[0069] II. seal coat comprising hydroxypropylmethyl cellulose;

[0070] III. extended release coating comprising: cellulose acetate, dibutyl sebacate, polyethylene glycol;

[0071] IV. sub coat comprising hydroxypropylmethyl cellulose; and

[0072] V. an immediate release coating comprising about 10 to 40% of pseudoephedrine hydrochloride by total weight of pseudoephedrine hydrochloride, and one or more other pharmaceutical excipients.

[0073] In an embodiment, the present invention provides a non-osmotic extended release formulation comprising pseudoephedrine or a salt thereof, comprising:

[0074] I. a core comprising: a) about 60% to 90% of pseudoephedrine or a salt thereof by total weight of pseudoephedrine or a salt thereof; b) a water soluble extended release polymer; and c) one or more other pharmaceutical excipients;

[0075] II. optional seal coat;

[0076] III. extended-release coating comprising: cellulose acetate, at least one plasticizer, at least one pore-former in the weight ratio of about 1:0.1:0.1 to 1:1.5:1.5;

[0077] IV. optional sub coat; and

[0078] V. an immediate release coating comprising about 10% to 40% of pseudoephedrine or a salt thereof by total weight of pseudoephedrine or a salt thereof, and one or more other pharmaceutical excipients.

[0079] In another embodiment, the present invention provides a non-osmotic extended release tablet comprising:

[0080] I. a core comprising: a) about 180 mg of pseudoephedrine hydrochloride; b) hydroxypropylmethyl cellulose; and c) one or more other pharmaceutical excipients;

[0081] II. optional seal coat;

[0082] III. extended release coating comprising: about 50% to 75% weight of cellulose acetate, and about 25% to 50% weight mixture of dibutyl sebacate and polyethylene glycol, by total weight of extended release coating composition, wherein the weight ratio of cellulose acetate, dibutyl sebacate and polyethylene glycol is from about 1:0.1:0.1 to 1:1:1;

[0083] IV. optional sub coat; and

[0084] V. an immediate release coating comprising about 60 mg of pseudoephedrine hydrochloride and hydroxypropylmethyl cellulose.

[0085] In yet another embodiment, the present invention provides a non-osmotic extended release tablet comprising

[0086] I. a core comprising: a) about 180 mg of pseudoephedrine hydrochloride; b) hydroxypropylmethyl cellulose; and c) one or more other pharmaceutical excipients;

[0087] II. optional seal coat;

[0088] III. extended release coating comprising: about 50% to 75% weight of cellulose acetate, and about 25% to 50% weight mixture of dibutyl sebacate and polyethylene glycol, by total weight of extended release coating composition, wherein the weight ratio of cellulose acetate, dibutyl sebacate and polyethylene glycol is about 1:0.15:0.3;

[0089] IV. optional sub coat; and

[0090] V. an immediate release coating comprising about 60 mg of pseudoephedrine hydrochloride and hydroxypropylmethyl cellulose.

[0091] In yet another embodiment, the present invention provides a non-osmotic extended release tablet comprising

[0092] I. a core comprising: a) about 180 mg of pseudoephedrine hydrochloride; b) hydroxypropylmethyl cellulose; and c) one or more other pharmaceutical excipients;

[0093] II. optional seal coat;

[0094] III. extended release coating comprising: about 50% to 75% weight of cellulose acetate, and about 25% to 50% weight mixture of dibutyl sebecate and polyethylene glycol, by total weight of extended release coating composition, wherein the weight ratio of cellulose acetate, dibutyl sebecate and polyethylene glycol is from about 1:0.1:0.1 to 1:0.3:0.5;

[0095] IV. optional sub coat; and

[0096] V. an immediate release coating comprising about 60 mg of pseudoephedrine hydrochloride and hydroxypropylmethyl cellulose; wherein an amount of pseudoephedrine hydrochloride released from the extended release tablet composition is from about 20% to 35% at 2 hours, from about 40% to 75% at 8 hours, from about 65% to 90% at 12 hours and not less than 85% at 24 hours.

[0097] In yet another embodiment, the present invention provides a non-osmotic extended release tablet comprising:

[0098] I. a core comprising: a) about 180 mg of pseudoephedrine hydrochloride; b) hydroxypropylmethyl cellulose; and c) one or more other pharmaceutical excipients;

[0099] II. optional seal coat;

[0100] III. extended release coating comprising: about 50% to 75% weight of cellulose acetate, and about 25% to 50% weight mixture of dibutyl sebecate and polyethylene glycol, by total weight of extended release coating composition, wherein the weight ratio of cellulose acetate, dibutyl sebecate and polyethylene glycol is from about 1:0.1:0.1 to 1:0.3:0.5;

[0101] IV. optional sub coat; and

[0102] V. an immediate release coating comprising about 60 mg of pseudoephedrine hydrochloride and hydroxypropylmethyl cellulose; wherein the extended release tablet has a comparative bioavailability profile with that of bioavailability profile of commercially available pseudoephedrine hydrochloride 240 mg extended release tablet.

[0103] In an embodiment, the present invention provides a non-osmotic extended release tablet comprising pseudoephedrine hydrochloride and cetirizine or levocetrizine or its salts thereof, comprising:

[0104] I. a tablet core comprising: a) about 60% to 90% of pseudoephedrine hydrochloride by total weight of pseudoephedrine hydrochloride; hydroxypropylmethyl cellulose; and c) one or more other pharmaceutical excipients;

[0105] II. seal coat comprising hydroxypropylmethyl cellulose;

[0106] III. extended release coating comprising: cellulose acetate, at least one plasticizer, at least one pore-former;

[0107] IV. sub coat comprising hydroxypropylmethyl cellulose; and

[0108] V. an immediate release coating comprising 10 to 40% of pseudoephedrine hydrochloride by total weight of pseudoephedrine hydrochloride, and about 1 to 10% of cetirizine or levocetrizine or its salts thereof, and one or more other pharmaceutical excipients.

[0109] In yet another embodiment, the present invention provides a non-osmotic extended release formulation comprising pseudoephedrine or a salt thereof, indicated for the relief of symptoms associated with nasal congestion in adults and children 12 years of age and older.

[0110] The following examples are intended to serve as illustrations of the present invention only and do not restrict the scope of the invention in any manner whatsoever.

EXAMPLES

Example 1

[0111] Non-osmotic extended release pseudoephedrine hydrochloride tablets 240 mg (matrix tablet with combination of HPMC polymers).

TABLE-US-00001 Ingredients Quantity/tablet (mg) Pseudoephedrine HCI 240.00 Hypromellose K 100M 380.00 Hypromellose E4M 100.00 Colloidal silicon dioxide 4.00 Stearic acid 8.00 Total 732.00

[0112] Brief manufacturing process: [0113] 1. Pseudoephedrine hydrochloride and other excipients (except stearic acid) were sifted separately in a suitable sieve and blended for appropriate time to get homogeneous unlubricated blend. [0114] 2. Blend of Step-1 was lubricated with stearic acid and compressed into tablets.

Example 2

[0115] Non-osmotic extended release pseudoephedrine hydrochloride tablets 240 mg (matrix tablet with combination of Hypromellose K100M in core & extended release coating membrane with a mixture of ethyl cellulose: Hypromellose—50:50)

TABLE-US-00002 Ingredients Quantity/tablet (mg) Core tablet Pseudoephedrine HCI 240.00 Hypromellose K 100M 195.00 Microcrystalline cellulose 17.00 Colloidal silicon dioxide 4.00 Stearic acid 8.00 Sub-total 464.00 Extended release coating Ethyl Cellulose 100 cps (EC) 41.76 Hypromellose E5 LV 41.76 Isopropyl alcohol/Dichloromethane Q.S. Purified Water Q.S. Total 547.52

[0116] Brief manufacturing process:

[0117] 1. Pseudoephedrine hydrochloride core tablets were prepared by direct compression like example 1 process.

[0118] 2. About 18% w/w of extended release coating were applied to core tablets of step 1.

Example 3

[0119] Non-osmotic extended release pseudoephedrine hydrochloride tablets 240 mg (matrix tablet with ethyl cellulose and hypromellose in core & extended release coating membrane with cellulose acetate).

TABLE-US-00003 Ingredients Quantity/tablet (mg) Core tablet prepared by Top-spray granulation Pseudoephedrine HCI 240.00 Ethyl cellulose 10 cps 48.00 Ethanol 96% Q.S. Purified water Q.S. HPMC K100M DC2 100.00 Colloidal silicon dioxide 4.00 Stearic acid 8.00 Sub-total 400.00 Seal Coating Opadry AMB II 88A180040 14.00 Sub-total 414.00 Extended release coating Cellulose acetate with suitable coating aids 24.84 (selected one plasticizer, atleast one pore- former, Acetone & purified water) Total 438.84

[0120] Brief manufacturing process:

[0121] 1. Blend was prepared by spraying hydro alcoholic solution of ethyl cellulose sprayed on to pseudoephedrine hydrochloride (top-spray technique).

[0122] 2. Dried granules of step-1 were blended with HPMC, colloidal silicon dioxide and lubricated with stearic acid.

[0123] 3. Lubricated blend of step-2 compressed into core tablets.

[0124] 4. Core tablets of step-3 were seal coated with aqueous dispersion of Opadry AMB II.

[0125] 5. Extended release coating was applied to core tablets of step 4.

Example 4

[0126] Non-osmotic extended release pseudoephedrine hydrochloride tablets 240 mg (matrix tablet with HPMC K100M & 240 mg of pseudoephedrine hydrochloride in core & 4.5% extended release membrane coating with cellulose acetate)

TABLE-US-00004 Ingredients Quantity/tablet (mg) Core tablet Pseudoephedrine HCI 240.00 Hypromellose K 100M 190.50 Lactose Monohydrate 4.50 Microcrystalline cellulose 17.00 Colloidal silicon dioxide 4.00 Stearic acid 8.00 Sub-Total 464.00 Seal Coating Opadry AMB II 88A180040 white 16.24 Purified Water Q.S. Sub-total 480.240 Extended release coating Cellulose acetate with suitable coating 21.611 aids (selected one plasticizer, atleast one pore-former, Acetone & purified water) Sub-total 501.851 Film Coating Opadry AMB II 88A180040 white 20.07 Purified Water Q.S. Total 521.92

[0127] Brief manufacturing process:

[0128] 1. Pseudoephedrine hydrochloride core tablets were prepared by direct compression like example 1 process.

[0129] 2. Seal coating: Aqueous dispersion of opadry AMB II white 88A180040 was sprayed onto the core tablets.

[0130] 3. Extended release coating: Hydroalcoholic dispersion of Cellulose acetate was sprayed onto the seal coated tablets.

[0131] 4. Film coating: Aqueous dispersion of opadry AMB II white 88A180040 was sprayed onto the extended release tablets.

Example 5

[0132] Non-osmotic extended release Pseudoephedrine hydrochloride tablets 240 mg (matrix tablet with HPMC K100M & 75% pseudoephedrine hydrochloride in core, 25% pseudoephedrine in immediate release coating & extended release coating with cellulose acetate)

TABLE-US-00005 Ingredients Quantity/tablet (mg) Core tablet Pseudoephedrine HCI 180.000 Hypromellose K 100M 157.875 Lactose Monohydrate 3.375 Microcrystalline cellulose 12.750 Colloidal silicon dioxide 3.000 Stearic acid 6.000 Sub-total 363.00 Seal coating Opadry AMB II 88A180040 white 12.705 Purified Water Q.S. Sub-total 375.705 Extended release coating Cellulose acetate with suitable coating aids 30.056 dibutyl sebacate and polyethylene glycol, in a ratio of 1:0.15:0.3 Sub-total 405.761 Sub coating Hypromellose 12.173 Purified Water Q.S. Sub-total 417.934 Immediate release drug loading Pseudoephedrine HCI 60.00 Hypromellose 10.00 Purified water Q.S. Sub-Total 487.934 Film coating Opadry AMB II 88A180040 white 19.517 Purified Water Q.S. Total 507.451

[0133] Brief manufacturing process:

[0134] 1. Pseudoephedrine hydrochloride core tablets were prepared by direct compression like example 1 process.

[0135] 2. Seal coating: Aqueous dispersion of opadry AMB II white 88A180040 was sprayed onto the core tablets.

[0136] 3. Extended release coating: Hydroalcoholic dispersion of Cellulose acetate with suitable coating aids (atleast plasticizer, atleast one pore-former, Acetone & purified water) was sprayed onto the seal coated tablets.

[0137] 4. Sub coating: Aqueous solution of Hypromellose was sprayed onto the extended release tablets.

[0138] 5. Immediate release coating (IR coating): Aqueous solution of drug and Hypromellose spray onto the sub coated tablets.

[0139] 6. Film coating: Aqueous dispersion of opadry AMB II white 88A180040 was sprayed onto the IR coated tablets of step-5.

Example 6

[0140] Cetirizine+Pseudoephedrine Non-osmotic extended release tablets (matrix tablet with HPMC K100M & 75% pseudoephedrine in core and 25% pseudoephedrine & 100% cetirizine in immediate release coating with extended release coating membrane of cellulose acetate)

TABLE-US-00006 Quantity/tablet Ingredients (mg) Core tablet Pseudoephedrine Hydrochloride 180.000 Hypromellose USP (Methocel K100M Premium DC2) 142.875 Lactose Monohydrate 3.380 Microcrystalline cellulose 12.750 Colloidal silicon dioxide 3.000 Stearic acid 6.000 Sub-total 348.000 Seal coating Opadry AMB II white 88A180040 12.180 Purified water 48.720 Sub-total 360.185 Extended release coating Cellulose acetate with suitable coating aids (selected one 28.81 plasticizer, at least one pore-former, Acetone & purified water) Sub-total 388.995 Sub coating Hypromellose (Methocel E3LV) 11.670 Purified water 182.827 Sub-total 400.665 Immediate release drug loading Pseudoephedrine Hydrochloride 60.000 Cetirizine Hydrochloride 10.000 Hypromellose USP (Methocel E3LV) 10.600 Disodium succinate Hexahydrate 14.627 Purified water 142.841 Sub-total 495.892 Film coating Opadry AMB II white 88A180040 19.836 Purified water USP.sup.@ 79.344 Total 515.728 Opacode Black S-1-17823 0.043

[0141] Brief manufacturing process:

[0142] 1. Pseudoephedrine hydrochloride core tablets were prepared by direct compression like example 1 process.

[0143] 2. Seal coating: Aqueous dispersion of opadry AMB II white 88A180040 was sprayed onto the core tablets.

[0144] 3. Extended release coating: Hydroalcoholic dispersion of Cellulose acetate was sprayed onto the seal coated tablets.

[0145] 4. Sub coating: Aqueous solution of Hypromellose was sprayed onto the extended release tablets.

[0146] 5. Immediate release coating (IR coating): Aqueous solution of pseudoephedrine hydrochloride, cetirizine hydrochloride and other excipients were sprayed onto the sub coated tablets.

[0147] 6. Film coating: Aqueous dispersion of opadry AMB II white 88A180040 was sprayed onto the IR coated tablets of step-5.

[0148] Experimental data:

[0149] In-Vitro dissolution study:

[0150] The release profile of the pharmaceutical composition comprising pseudoephedrine hydrochloride as per the present specification was evaluated through in-vitro dissolution studies. The compositions were prepared according to the formula and process of examples 1-5 and were subjected to an in-vitro dissolution study in 900 ml of 0.001N HCl, at a temperature of 37±0.5° C. using a USP apparatus-2 (paddle) with sinker at a rotation of about 50 rpm and results are given in Table-1 below:

TABLE-US-00007 TABLE 1 Comparative dissolution profile: Time Points % Drug Release (hour) SUDAFED Example 1 Example 2 Example 3 Example 4 Example 5 0.5 25 — — —  0 25 1 26 29  0  0  0 26 2 29 — — —  3 26 3 — 53  2  2 — 4 35 — — — 19 29 5 — 83 17 12 — 6 43 — — — 36 37 7 — — 39 36 — 8 53 — — — 51 51 9 — — 60 58 — — 10 63 — — — 66 62 11 — — 77 72 — — 12 72 — — — 75 71 13 — — — 81 — — 14 80 — — — 82 77 15 — — — 86 — — 16 85 — — — 86 82 17 — — — 89 — — 18 89 — — — 90 86 20 92 — — — 91 88 22 94 — — — 93 90 23 — — — 95 — — 24 96 — — — 95 92

[0151] The extended release pseudoephedrine hydrochloride tablets 240 mg of example-5 with an unexpected combination of a rate controlling core with an extended release coating system comprising cellulose acetate, dibutyl sebacate, and polyethylene glycol in a ratio of 1:0.15: 0.3, gave comparative dissolution profile with that of SUDAFED® 24 HOUR (pseudoephedrine hydrochloride ER tablets 240 mg).

Examples 7-8

[0152] Non-osmotic extended release pseudoephedrine hydrochloride tablets 240 mg (matrix tablet with HPMC K100M & 75% Pseudoephedrine hydrochloride in core, 25% Pseudoephedrine in immediate release coating & extended release coating with cellulose acetate:plasticizer:pore former in different ratios)

TABLE-US-00008 Example 7 Example 8 Ingredients Quantity/tablet (mg) Core tablet Pseudoephedrine HCI 180 180 Hypromellose K 100M 157.875 142.875 Lactose Monohydrate 3.375 3.375 Microcrystalline cellulose 12.75 12.75 Colloidal silicon dioxide 3 3 Stearic acid 6 6 Sub-total 363 348 Seal coating Opadry AMB II 88A180040 white 12.705 12.18 Purified Water Q.S. 48.72 Sub-total 375.705 360.18 Extended release coating Cellulose acetate 9.393 18.009 Dibutyl Sebacate 10.332 1.801 Polyethylene glycol 400 10.332 3.602 Ratio of Cellulose acetate: 1:1.1:1.1 1:0.1:0.2 plasticizer:pore-former Sub-total 405.762 383.592 Sub coating Hypromellose 12.173 11.508 Purified Water Q.S. 182.827 Sub-total 417.935 395.1 Immediate release drug loading Pseudoephedrine HCI 60 60 Hypromellose 10 10.6 Purified water Q.S. QS Sub-Total 487.935 465.7 Film coating Opadry AMB II 88A180040 white 19.516 18.628 Purified Water Q.S. QS Total 507.451 484.32

[0153] Brief manufacturing process: [0154] 1. Pseudoephedrine hydrochloride core tablets were prepared Examples 7-8 were prepared same as example 5.

[0155] In-vitro dissolution study:

[0156] The release profile of the pharmaceutical composition comprising pseudoephedrine HCl as per the present specification was evaluated through in-vitro dissolution studies. The composition was prepared according to the formula and process of examples 7 & 8 and was subjected to an in vitro dissolution study in 900 ml of 0.001N HCl, at a temperature of 37 0.5° C. using a USP apparatus-2 (paddle) with sinker at a rotation of about 50 rpm and results are given in Table-2 below:

TABLE-US-00009 TABLE 2 Comparative dissolution profile: % Drug Release Time Points (hour) Example 7 Example 8 2 28 26 8 67 52 12 84 73 24 97 96 F2 factor compared with 67 67 SUDAFED ® 24 HOUR

[0157] Surprisingly, extended release pseudoephedrine hydrochloride tablets 240 mg of examples 7-8 with an unexpected combination of a rate controlling core with an extended release coating system comprising cellulose acetate, dibutyl sebacate, polyethylene glycol in a ratio of 1:1.1:1.1 to 1:0.1:0.2, gave comparative dissolution with that of SUDAFED®24 HOUR (Pseudoephedrine Hydrochloride ER tablets 240 mg).

[0158] Comparative Bioequivalence Data: “Reference Product” [SUDAFED® ER Tablets] Versus “Test Product” [Pseudoephedrine HCl ER Tablets].

[0159] A randomized, two-treatment, two-sequence, two-period, crossover, single-dose oral Bioequivalence study of Pseudoephedrine Hydrochloride Extended-Release tablets (Test) of Aurobindo Pharma Limited example 5 and SUDAFED® 24 HOUR (Pseudoephedrine Hydrochloride ER tablets) (Reference) of Johnson & Johnson consumer Inc., USA in healthy, adult, human subjects under fasting and fed condition. T/R (Test/Reference) ratio results are as follows:—

TABLE-US-00010 Acceptable T/R Ratio Parameters limit (Test - Example 5) Cmax/AUCI 0-t/AUC 0-inf - Fasting 80-125 Within the acceptable limit Cmax/AUCI 0-t/AUC 0-inf - Fed 80-125 Within the acceptable limit

[0160] Based on above T/R ratio, it was surprisingly found that Test product of example 5 results were well within the acceptable limits and was bio-equivalent to the Reference product.

[0161] Surprisingly, extended release Pseudoephedrine hydrochloride tablets 240mg of example-5 with an unexpected combination of a rate controlling core with an extended release coating system comprising cellulose acetate, dibutyl sebacate, and polyethylene glycol in a ratio of 1:0.15:0.3, gave comparative dissolution & bioavailability profiles with that of SUDAFED® 24 HOUR (Pseudoephedrine Hydrochloride ER tablets 240 mg).