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

Microbeads of diltiazem, a process for their manufacture and a substained-release pharmaceutical composition containing them

Patent 5344657 Issued on September 6, 1994. Estimated Expiration Date: Icon_subject April 5, 2013. 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

Pharmaceutical compositions in the form of beadlets and method
Patent #: 4808413
Issued on: 02/28/1989
Inventor: Joshi ,   et al.

Controlled absorption diltiazem formulation for once-daily administration
Patent #: 4894240
Issued on: 01/16/1990
Inventor: Geoghegan, et al.

Controlled absorption diltiazem formulation
Patent #: 4917899
Issued on: 04/17/1990
Inventor: Geoghegan, et al.

Coating membrane and compositions prepared therefrom Patent #: 5149542
Issued on: 09/22/1992
Inventor: Valducci

Inventor

Assignee

Application

No. 043592 filed on 04/05/1993

US Classes:

424/458, Containing discrete coated particles pellets, granules, or beads424/451, Capsules (e.g., of gelatin, of chocolate, etc.)424/459Organic coatings

Examiners

Primary: Page, Thurman K.
Assistant: Benston, William E. Jr.

Attorney, Agent or Firm

Foreign Patent References

  • 0099109 EP. 01/13/1984
  • 0149920 EP. 07/13/1985
  • 0207041 EP. 12/13/1986
  • 0216743 EP. 04/13/1987
  • 2091203 GB. 07/13/1982

International Class

A61K 009/54

Foreign Application Priority Data

1988-04-27 FR

Abstract

The microbeads are composed of a core containing the active ingredient and a microporous membrane, insoluble in aqueous medium, consisting of a film-forming polymer, a plasticizer and a filling material.The membrane has a thickness such that diltiazem is released in vitro at an approximately constant rate for at least 6 hours after a latent period of less than one hour.The active ingredient can be intimately mixed with the core or included in a polyvinyl pyrrolidone layer coating an inert grain.The sustained-release microbeads are formed by application to the core of a dispersion of the constituents of the membrane in a solvent and evaporation of the solvent.The pharmaceutical compositions consist of capsules containing the microbeads. They are administered orally one or twice per day, depending on the dose, for the treatment of angina or hypertension.

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