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

Sustained-release formulations

Patent 5055306 Issued on October 8, 1991. Estimated Expiration Date: Icon_subject October 20, 2008. 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

3131123

Effervescent enteric coated L-dopa formulation and method of using the same
Patent #: 3961041
Issued on: 06/01/1976
Inventor: Nishimura ,   et al.

Enteric coated digoxin and therapeutic use thereof
Patent #: 4147768
Issued on: 04/03/1979
Inventor: Shaffer ,   et al.

Indicator device in an inverted Galilean finder
Patent #: 4348091
Issued on: 09/07/1982
Inventor: Iizuka

Amosulalol hydrochloride long acting formulations
Patent #: 4765988
Issued on: 08/23/1988
Inventor: Sonobe ,   et al.

Pharmaceutical preparation for oral use
Patent #: 4786505
Issued on: 11/22/1988
Inventor: Lovgren ,   et al.

Disintegrating tablet and process for its preparation
Patent #: 4832956
Issued on: 05/23/1989
Inventor: Gergely ,   et al.

Granule remaining in stomach Patent #: 4844905
Issued on: 07/04/1989
Inventor: Ichikawa ,   et al.

Inventors

Assignee

Application

No. 260415 filed on 10/20/1988

US Classes:

424/482, Containing solid synthetic polymers424/466, Effervescent424/480Cellulose or derivative

Examiners

Primary: Page, Thurman K.
Assistant: Hulina, Amy

Attorney, Agent or Firm

Foreign Patent References

  • 0052076 EP. 11/12/1980
  • 0207041 EP. 06/12/1986
  • 0255404 EP. 07/12/1987
  • 2086725 GB. 11/12/1981

International Classes

A61K 009/32
A61K 009/46
A61K 007/36

Foreign Application Priority Data

1987-10-22 GB

Abstract

A granular sustained-release formulation of a pharmacologically active substance presented in the form of a tablet, said tablet comprising sufficient granules to provide a predetermined dose or number of doses of the pharmacologically active substance and effervescent or water-dispersible ingredients, each of said granules having a diameter of preferably between 0.5 and 2.5 mm and comprising:a) a core comprising one or more pharmacologically active substances and preferably one or more excipients; andb) a coating covering substantially the whole surface of the core and comprising 100 parts of a water insoluble but water swellable acrylic polymer and from 20 to 70 parts of a water soluble hydroxylated cellulose derivative, the weight of the coating being from 2 to 25% of the weight of the core.A method for preparing this effervescent of water-dispersible tablet formulation is also provided. Such formulations enable large dosages in sustained-release form to be more easily administered to patients.

Other References

  • "Eudragit.RTM. NE30D" Technical Application Pamphlet, Aqueous Dispersion for Controlled-Release Permeable Film Coating
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