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US4521402A Expired / Lapsed US ⏱️ 0.0 years remaining

Constant release rate solid oral dosage formulations of hydrazine

Assignee: Verex Laboratories Inc
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Filing: 1984-02-17
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Granted: 1985-06-04
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Expires: 2004-02-17
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Abstract

Abstract A constant order release rate solid oral dosage formulation of hydralazine or a pharmaceutically acceptable salt thereof, said formulation comprising: a therapeutically effective amount of hydralazine or a pharmaceutically acceptable salt; from about 0.5 to 6.0 weight percent of an acid-retardant or hydrophobic cellulose derivative; from about 2.5 to 35 weight percent of a hydrogenated vegetable oil: from about 1 to 20 weight percent of an acrylic acid polymer; from about 0.5 to 4.0 weight percent of fumed silicon dioxide and from about 0.4 to 3.0 percent of a lubricant.

Inventors

  • 👤 James M. Dunn

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-29 12:35
CPC Classifications
A; A61; A61K; A61K31/00; A61K31/275; A61K9/00; A61K9/20; A61K9/2004; A61K9/2009; A61K9/2013; A61K9/2022; A61K9/2027; A61K9/205; A61K9/2054

Claims Analysis

Total Claims: 11
Claim 1
Independent Claim 104 words
A constant order release solid oral dosage formulation of hydralazine or a pharmaceutically acceptable salt thereof, said formulation comprising: a therapeutically effective amount of hydralazine or a phramaceutically acceptable salt thereof; from about 0.5 to 6.0 weight percent of one or more cellulose derivatives selected from the group consisting of cellulose acetate phthalate, hydroxypropylmethylcellulose, phthalate ethyl cellulose, and microcrystalline cellulose; from about 2.5 to 35 weight percent of a hydrogenated vegetable oil; from about 1 to 20 weight percent of carboxypolymethylene; from about 0.5 to 4.0 weight percent of fumed silicon dioxide and from about 0.4 to 3.0 weight percent of a tabletting lubricant.
Claim 2
Dependent Claim 104 words
A constant order release solid oral dosage formulation of hydralazine or a pharmaceutically acceptable salt thereof, said formulation comprising: a therapeutically effective amount of hydralazine or a phramaceutically acceptable salt thereof; from about 0.5 to 6.0 weight percent of one or more cellulose derivatives selected from the group consisting of cellulose acetate phthalate, hydroxypropylmethylcellulose, phthalate ethyl cellulose, and microcrystalline cellulose; from about 2.5 to 35 weight percent of a hydrogenated vegetable oil; from about 1 to 20 weight percent of carboxypolymethylene; from about 0.5 to 4.0 weight percent of fumed silicon dioxide and from about 0.4 to 3.0 weight percent of a tabletting lubricant.
Claim 3
Dependent Claim 19 words
The formulation of claim 1 wherein said cellulose derivative is a combination of cellulose acetate phthalate and microcrystalline cellulose.
Claim 4
Dependent Claim 14 words
The formulation of claim 1 wherein said hydrogenated vegetable oil is hydrogenated cottonseed oil.
Claim 5
Dependent Claim 12 words
The formulation of claim 1 wherein said cellulose derivative is microcrystalline cellulose.
Claim 6
Dependent Claim 28 words
The formulation of claim 1 wherein said cellulose derivative is a combination of cellulose acetate phthalate and microcrystalline cellulose, and said hydrogenated vegetable oil is hydrogenated cottonseed oil.
Claim 7
Dependent Claim 21 words
The formulation of claim 1 wherein said cellulose derivative is microcrystalline cellulose and said hydrogenated vegetable oil is hydrogenated cottonseed oil.
Claim 8
Dependent Claim 89 words
A constant order release solid oral dosage formulation of hydralazine or a pharmaceutically acceptable salt thereof comprising: a therapeutically effective amount of hydralazine or a pharmaceutically acceptable salt thereof; from 0.5 to 6.0 weight percent of a combination of microcrystalline cellulose and cellulose acetate phthalate; from about 2.5 to 35 weight percent of a hydrogenated vegetable oil; from about 1 to 20 weight percent of carboxypolymethylene; from about 0.5 to 4.0 weight percent of fumed silicon dioxide and from about 0.4. to 3.0 weight percent of a tabletting lubricant.
Claim 9
Dependent Claim 89 words
A constant order release solid oral dosage formulation of hydralazine or a pharmaceutically acceptable salt thereof comprising: a therapeutically effective amount of hydralazine or a pharmaceutically acceptable salt thereof; from 0.5 to 6.0 weight percent of a combination of microcrystalline cellulose and cellulose acetate phthalate; from about 2.5 to 35 weight percent of a hydrogenated vegetable oil; from about 1 to 20 weight percent of carboxypolymethylene; from about 0.5 to 4.0 weight percent of fumed silicon dioxide and from about 0.4. to 3.0 weight percent of a tabletting lubricant.
Claim 10
Dependent Claim 84 words
A constant order release solid oral dosage formulation of hydralazine of a pharmaceutically acceptable salt thereof comprising: a therapeutically effective amount of hydralazine or a pharmaceutically acceptable salt thereof; from 0.5 to 6.0 weight percent of ethyl cellulose; from about 2.5 to 35 weight percent of a hydrogenated vegetable oil; from about 1 to 20 weight percent of carboxypolymethylene; from about 0.5 to 4.0 weight percent of fumed silicon dioxide; and from about 0.4 to 3.0 weight percent of a pharmaceutically acceptable tabletting lubricant.
Claim 11
Dependent Claim 84 words
A constant order release solid oral dosage formulation of hydralazine of a pharmaceutically acceptable salt thereof comprising: a therapeutically effective amount of hydralazine or a pharmaceutically acceptable salt thereof; from 0.5 to 6.0 weight percent of ethyl cellulose; from about 2.5 to 35 weight percent of a hydrogenated vegetable oil; from about 1 to 20 weight percent of carboxypolymethylene; from about 0.5 to 4.0 weight percent of fumed silicon dioxide; and from about 0.4 to 3.0 weight percent of a pharmaceutically acceptable tabletting lubricant.

References Cited (Backward Citations)

US3400197A Cited
US4248856A Cited
US4248858A Cited
US4248857A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1988-06-03 1988-12-03 1989-06-04 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1992-06-03 1992-12-03 1993-06-04 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1996-06-03 1996-12-03 1997-06-04 $7700.00 Window Closed / Lapsed

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