Wednesday 15 June 2011

Depakote


See also: Generic Depakote ER


Depakote is a brand name of divalproex sodium, approved by the FDA in the following formulation(s):


DEPAKOTE (divalproex sodium - capsule, delayed rel pellets; oral)



  • Manufacturer: ABBOTT

    Approval date: September 12, 1989

    Strength(s): EQ 125MG VALPROIC ACID [RLD][AB]

DEPAKOTE (divalproex sodium - tablet, delayed release; oral)



  • Manufacturer: ABBOTT

    Approval date: March 10, 1983

    Strength(s): EQ 250MG VALPROIC ACID [AB], EQ 500MG VALPROIC ACID [RLD][AB]


  • Manufacturer: ABBOTT

    Approval date: October 26, 1984

    Strength(s): EQ 125MG VALPROIC ACID [AB]

Has a generic version of Depakote been approved?


A generic version of Depakote 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 Depakote and have been approved by the FDA:


divalproex sodium capsule, delayed rel pellets; oral



  • Manufacturer: DR REDDYS LABS LTD

    Approval date: January 23, 2009

    Strength(s): EQ 125MG VALPROIC ACID [AB]


  • Manufacturer: MYLAN

    Approval date: March 28, 2011

    Strength(s): EQ 125MG VALPROIC ACID [AB]


  • Manufacturer: ZYDUS PHARMS USA INC

    Approval date: January 27, 2009

    Strength(s): EQ 125MG VALPROIC ACID [AB]

divalproex sodium tablet, delayed release; oral



  • Manufacturer: ANCHEN PHARMS

    Approval date: November 3, 2008

    Strength(s): EQ 500MG VALPROIC ACID [AB]


  • Manufacturer: AUROBINDO PHARMA LTD

    Approval date: April 21, 2011

    Strength(s): EQ 125MG VALPROIC ACID [AB], EQ 250MG VALPROIC ACID [AB], EQ 500MG VALPROIC ACID [AB]


  • Manufacturer: DR REDDYS LABS LTD

    Approval date: July 29, 2008

    Strength(s): EQ 125MG VALPROIC ACID [AB], EQ 250MG VALPROIC ACID [AB], EQ 500MG VALPROIC ACID [AB]


  • Manufacturer: LUPIN

    Approval date: July 29, 2008

    Strength(s): EQ 125MG VALPROIC ACID [AB], EQ 250MG VALPROIC ACID [AB], EQ 500MG VALPROIC ACID [AB]


  • Manufacturer: MYLAN

    Approval date: July 29, 2008

    Strength(s): EQ 125MG VALPROIC ACID [AB], EQ 250MG VALPROIC ACID [AB], EQ 500MG VALPROIC ACID [AB]


  • Manufacturer: MYLAN

    Approval date: March 17, 2009

    Strength(s): EQ 125MG VALPROIC ACID [AB], EQ 250MG VALPROIC ACID [AB], EQ 500MG VALPROIC ACID [AB]


  • Manufacturer: NU PHARM

    Approval date: July 29, 2008

    Strength(s): EQ 125MG VALPROIC ACID [AB], EQ 250MG VALPROIC ACID [AB], EQ 500MG VALPROIC ACID [AB]


  • Manufacturer: ORCHID HLTHCARE

    Approval date: November 25, 2008

    Strength(s): EQ 125MG VALPROIC ACID [AB], EQ 250MG VALPROIC ACID [AB], EQ 500MG VALPROIC ACID [AB]


  • Manufacturer: SANDOZ

    Approval date: July 29, 2008

    Strength(s): EQ 125MG VALPROIC ACID [AB], EQ 250MG VALPROIC ACID [AB], EQ 500MG VALPROIC ACID [AB]


  • Manufacturer: SUN PHARM INDS

    Approval date: July 29, 2008

    Strength(s): EQ 125MG VALPROIC ACID [AB], EQ 250MG VALPROIC ACID [AB], EQ 500MG VALPROIC ACID [AB]


  • Manufacturer: TEVA

    Approval date: July 29, 2008

    Strength(s): EQ 125MG VALPROIC ACID [AB], EQ 250MG VALPROIC ACID [AB], EQ 500MG VALPROIC ACID [AB]


  • Manufacturer: UNICHEM LABS LTD

    Approval date: April 5, 2011

    Strength(s): EQ 125MG VALPROIC ACID [AB], EQ 250MG VALPROIC ACID [AB], EQ 500MG VALPROIC ACID [AB]


  • Manufacturer: UPSHER SMITH

    Approval date: July 29, 2008

    Strength(s): EQ 125MG VALPROIC ACID [AB], EQ 250MG VALPROIC ACID [AB], EQ 500MG VALPROIC ACID [AB]


  • Manufacturer: VINTAGE

    Approval date: November 30, 2009

    Strength(s): EQ 125MG VALPROIC ACID [AB], EQ 250MG VALPROIC ACID [AB], EQ 500MG VALPROIC ACID [AB]


  • Manufacturer: WATSON LABS FLORIDA

    Approval date: February 25, 2011

    Strength(s): EQ 500MG VALPROIC ACID [AB]


  • Manufacturer: WOCKHARDT

    Approval date: July 31, 2008

    Strength(s): EQ 125MG VALPROIC ACID [AB], EQ 250MG VALPROIC ACID [AB], EQ 500MG VALPROIC ACID [AB]


  • Manufacturer: ZYDUS PHARMS USA INC

    Approval date: March 5, 2009

    Strength(s): EQ 125MG VALPROIC ACID [AB], EQ 250MG VALPROIC ACID [AB], EQ 500MG VALPROIC ACID [AB]

Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Depakote. 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 Depakote.

Related Exclusivities

Exclusivity is exclusive marketing rights granted by the FDA upon approval of a drug and can run concurrently with a patent or not. Exclusivity is a statutory provision and is granted to an NDA applicant if statutory requirements are met.

  • Exclusivity expiration dates:
    • March 24, 2011 - EXPANDED INFORMATION TO PEDIATRIC USE SUBSECTION OF LABELING IN RESPONSE TO PEDIATRIC WRITTEN REQUEST

    • September 24, 2011 - PEDIATRIC EXCLUSIVITY

See also...

  • Depakote Consumer Information (Drugs.com)
  • Depakote Delayed-Release Tablets Consumer Information (Wolters Kluwer)
  • Depakote Sprinkle Capsules Consumer Information (Wolters Kluwer)
  • Depakote Consumer Information (Cerner Multum)
  • Depakote Advanced Consumer Information (Micromedex)
  • Divalproex Delayed-Release Tablets Consumer Information (Wolters Kluwer)
  • Divalproex Extended-Release Tablets Consumer Information (Wolters Kluwer)
  • Divalproex Sprinkle Capsules Consumer Information (Wolters Kluwer)
  • Divalproex sodium Consumer Information (Cerner Multum)
  • Alti-Valproic Advanced Consumer Information (Micromedex)
  • Depakote DR Advanced Consumer Information (Micromedex)
  • Divalproex sodium Advanced Consumer Information (Micromedex)

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