U.S. patents available from 1976 to present.
U.S. patent applications available from 2005 to present.

Compositions containing ibuprofen

Patent 4837031 Issued on June 6, 1989. Estimated Expiration Date: Icon_subject September 17, 2007. Estimated Expiration Date is calculated based on simple USPTO term provisions. It does not account for terminal disclaimers, term adjustments, failure to pay maintenance fees, or other factors which might affect the term of a patent.

Patent References

L-ascorbic acid tablets
Patent #: 4036948
Issued on: 07/19/1977
Inventor: Kitamori ,   et al.

Directly compressible acetaminophen granulation
Patent #: 4439453
Issued on: 03/27/1984
Inventor: Vogel

Aspirin tablet
Patent #: 4555399
Issued on: 11/26/1985
Inventor: Hsiao

Process for preparing granulate containing poorly compressible medicinally active matter
Patent #: 4562024
Issued on: 12/31/1985
Inventor: Rogerson

Stable, high dose, high bulk density ibuprofen granulations for tablet and capsule manufacturing
Patent #: 4609675
Issued on: 09/02/1986
Inventor: Franz

Direct tableting acetaminophen compositions Patent #: 4661521
Issued on: 04/28/1987
Inventor: Salpekar ,   et al.

Inventor

Application

No. 07/097850 filed on 09/17/1987

US Classes:

424/464, Tablets, lozenges, or pills424/465, With claimed perfecting feature in contents (e.g., excipient, lubricant, etc.)424/490, Coated (e.g., microcapsules)424/492, Gelatin424/494, Cellulose derivatives424/497Containing solid synthetic polymers

Examiners

Primary: Dixon, William R. Jr.
Assistant: Brunsman, David

Attorney, Agent or Firm

International Classes

A61K 9/16 (20060101)
A61K 9/20 (20060101)
A61K 31/19 (20060101)
A61K 31/185 (20060101)

Abstract

A granular composition containing 2-(4-isobutylphenyl)propionic acid (ibuprofen) as an active anti-inflammatory pharmaceutical ingredient as a major component, together with carboxymethylcellulose, a lubricant and water as minor components, is disclosed. Particles of ibuprofen and carboxymethylcellulose are both fluidized and coated with an aqueous disperson of a starch binder. After being dried to a moisture level of about 1-5% and blended with a lubricant and additional carboxymethylcellulose, the resulting granules can be directly molded into a pharmaceutically acceptable tablet having high hardness, short disintegration time and fast dissolution rate.

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