Wednesday, May 27, 2009

Aricept ODT


See also: Generic Aricept


Aricept ODT is a brand name of donepezil, approved by the FDA in the following formulation(s):


ARICEPT ODT (donepezil hydrochloride - tablet, orally disintegrating; oral)



  • Manufacturer: EISAI INC

    Approval date: October 18, 2004

    Strength(s): 10MG [RLD][AB], 5MG [AB]

Has a generic version of Aricept ODT been approved?


A generic version of Aricept ODT has been approved by the FDA. However, this does not mean that the product will necessarily be commercially available - possibly because of drug patents and/or drug exclusivity. The following products are equivalent to Aricept ODT and have been approved by the FDA:


donepezil hydrochloride tablet, orally disintegrating; oral



  • Manufacturer: BARR

    Approval date: November 26, 2010

    Strength(s): 10MG [AB], 5MG [AB]


  • Manufacturer: SANDOZ

    Approval date: May 10, 2011

    Strength(s): 10MG [AB], 5MG [AB]


  • Manufacturer: ZYDUS PHARMS USA INC

    Approval date: May 10, 2011

    Strength(s): 10MG [AB], 5MG [AB]

Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Aricept ODT. These medications may be counterfeit and potentially unsafe. If you purchase medications online, be sure you are buying from a reputable and valid online pharmacy. Ask your health care provider for advice if you are unsure about the online purchase of any medication.

See also: About generic drugs.




Related Patents


Patents are granted by the U.S. Patent and Trademark Office at any time during a drug's development and may include a wide range of claims.




  • Rapidly disintegrable tablet containing polyvinyl alcohol
    Patent 7,727,548
    Issued: June 1, 2010
    Inventor(s): Morita; Yutaka & Yasui; Masanobu & Ohwaki; Takayuki & Tsushima; Yuki
    Assignee(s): Eisai R&D Management Co., Ltd.
    The present invention provides a quickly disintegrating tablet which has quick disintegrability and solubility in an oral cavity, and does not have uncomfortable tastes such as bitterness, has a small variation of a tablet physical property even in storage under a humidifying condition, and has substantially no change in a medicine content in the tablet and tablet appearance and which is superior in stability; and a manufacturing method of the tablet. That is, it provides: a quickly disintegrating tablet which is prepared by blending a medicine with a saccharide and polyvinyl alcohol, which has small variations of tablet weight, tablet hardness, tablet diameter and tablet thickness, and which is superior in medicine stability in the tablet; and a manufacturing method of the tablet.
    Patent expiration dates:

    • June 23, 2022
      ✓ 
      Patent use: ADMINISTRATION OF APPROVED PRODUCT FOR TREATMENT OF ALZHEIMER'S DISEASE
      ✓ 
      Drug product




  • Oral pharmaceutical preparations decreased in bitterness by masking
    Patent 7,727,552
    Issued: June 1, 2010
    Inventor(s): Ukai; Koji & Hrada; Tsutomu & Suzuki; Yasuyuki
    Assignee(s): Eisai R&D Management Co., Ltd.
    A composition of an oral medicine or an oral medicine which can prevent an unpleasant taste of the medicine is herein disclosed. It is granules, powders, syrups and the like which is prevented from an unpleasant taste, comprising a basic medicine having an unpleasant taste and an anionic polymer such as carrageenan.
    Patent expiration dates:

    • March 26, 2018
      ✓ 
      Drug product



See also...

  • Aricept ODT Orally Disintegrating Tablets Consumer Information (Wolters Kluwer)
  • Aricept ODT Consumer Information (Cerner Multum)
  • Donepezil Consumer Information (Wolters Kluwer)
  • Donepezil Orally Disintegrating Tablets Consumer Information (Wolters Kluwer)
  • Donepezil Consumer Information (Cerner Multum)
  • Donepezil Advanced Consumer Information (Micromedex)
  • Donepezil Hydrochloride AHFS DI Monographs (ASHP)

Apo-Tenoxicam




Apo-Tenoxicam may be available in the countries listed below.


Ingredient matches for Apo-Tenoxicam



Tenoxicam

Tenoxicam is reported as an ingredient of Apo-Tenoxicam in the following countries:


  • Canada

  • Vietnam

International Drug Name Search

Sunday, May 24, 2009

Vantas


Vantas is a brand name of histrelin, approved by the FDA in the following formulation(s):


VANTAS (histrelin acetate - implant; subcutaneous)



  • Manufacturer: ENDO PHARM

    Approval date: October 12, 2004

    Strength(s): 50MG [RLD]

Has a generic version of Vantas been approved?


No. There is currently no therapeutically equivalent version of Vantas available.


Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Vantas. These medications may be counterfeit and potentially unsafe. If you purchase medications online, be sure you are buying from a reputable and valid online pharmacy. Ask your health care provider for advice if you are unsure about the online purchase of any medication.

See also: About generic drugs.




Related Patents

There are no current U.S. patents associated with Vantas.

See also...

  • Vantas Consumer Information (Drugs.com)
  • Vantas Implant Consumer Information (Wolters Kluwer)
  • Vantas implant Consumer Information (Cerner Multum)
  • Vantas Advanced Consumer Information (Micromedex)
  • Vantas AHFS DI Monographs (ASHP)
  • Supprelin-LA Consumer Information (Drugs.com)
  • Histrelin Implant Consumer Information (Wolters Kluwer)
  • Histrelin implant Consumer Information (Cerner Multum)
  • Histrelin Subcutaneous Advanced Consumer Information (Micromedex)
  • Histrelin acetate Subcutaneous Advanced Consumer Information (Micromedex)
  • Histrelin AHFS DI Monographs (ASHP)

Wednesday, May 20, 2009

Antobron




Antobron may be available in the countries listed below.


Ingredient matches for Antobron



Ambroxol

Ambroxol hydrochloride (a derivative of Ambroxol) is reported as an ingredient of Antobron in the following countries:


  • Japan

International Drug Name Search

Tuesday, May 19, 2009

Retin-A


Retin-A is a brand name of tretinoin topical, approved by the FDA in the following formulation(s):


RETIN-A (tretinoin - cream; topical)



  • Manufacturer: VALEANT INTL

    Approved Prior to Jan 1, 1982

    Strength(s): 0.05% [RLD][AB1], 0.1% [RLD][AB]


  • Manufacturer: VALEANT INTL

    Approval date: September 16, 1988

    Strength(s): 0.025% [RLD][AB]

RETIN-A (tretinoin - gel; topical)



  • Manufacturer: VALEANT INTL

    Approved Prior to Jan 1, 1982

    Strength(s): 0.01% [RLD][AB], 0.025% [RLD][AB]

RETIN-A (tretinoin - solution; topical)



  • Manufacturer: VALEANT INTL

    Approved Prior to Jan 1, 1982

    Strength(s): 0.05% [RLD][AT]

Has a generic version of Retin-A been approved?


Yes. The following products are equivalent to Retin-A:


AVITA (tretinoin cream; topical)



  • Manufacturer: MYLAN BERTEK

    Approval date: January 14, 1997

    Strength(s): 0.025% [AB]

tretinoin cream; topical



  • Manufacturer: TRIAX PHARMS LLC

    Approval date: December 24, 1998

    Strength(s): 0.025% [AB], 0.05% [AB1], 0.1% [AB]

tretinoin gel; topical



  • Manufacturer: TRIAX PHARMS LLC

    Approval date: February 22, 2000

    Strength(s): 0.025% [AB]


  • Manufacturer: TRIAX PHARMS LLC

    Approval date: June 11, 2002

    Strength(s): 0.01% [AB]

tretinoin solution; topical



  • Manufacturer: WOCKHARDT

    Approval date: January 25, 1999

    Strength(s): 0.05% [AT]

Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Retin-A. These medications may be counterfeit and potentially unsafe. If you purchase medications online, be sure you are buying from a reputable and valid online pharmacy. Ask your health care provider for advice if you are unsure about the online purchase of any medication.

See also: About generic drugs.




Related Patents

There are no current U.S. patents associated with Retin-A.

See also...

  • Retin-A Cream Consumer Information (Wolters Kluwer)
  • Retin-A Gel Consumer Information (Wolters Kluwer)
  • Retin-A Liquid Consumer Information (Wolters Kluwer)
  • Retin-A Consumer Information (Cerner Multum)
  • Retin-A Topical Advanced Consumer Information (Micromedex)
  • Retin A Consumer Information (Drugs.com)
  • Tretinoin Cream Consumer Information (Wolters Kluwer)
  • Tretinoin Emollient Cream Consumer Information (Wolters Kluwer)
  • Tretinoin Gel Consumer Information (Wolters Kluwer)
  • Tretinoin Liquid Consumer Information (Wolters Kluwer)
  • Tretinoin topical Consumer Information (Cerner Multum)
  • Rejuva-A Topical Advanced Consumer Information (Micromedex)
  • Retin-A Micro Topical Advanced Consumer Information (Micromedex)
  • Vitamin A Acid Topical Advanced Consumer Information (Micromedex)
  • Tretinoin Topical Advanced Consumer Information (Micromedex)
  • Tretinoin topical AHFS DI Monographs (ASHP)

Saturday, May 16, 2009

Zanidion




Zanidion may be available in the countries listed below.


Ingredient matches for Zanidion



Codeine

Codeine phosphate hemihydrate (a derivative of Codeine) is reported as an ingredient of Zanidion in the following countries:


  • Vietnam

Paracetamol

Paracetamol is reported as an ingredient of Zanidion in the following countries:


  • Vietnam

International Drug Name Search

Thursday, May 14, 2009

Microsona




Microsona may be available in the countries listed below.


Ingredient matches for Microsona



Hydrocortisone

Hydrocortisone is reported as an ingredient of Microsona in the following countries:


  • Argentina

  • Mexico

International Drug Name Search