DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
DIVALPROEX
FDA Application No:
(ANDA) 077296
Active Ingredient(s):
DIVALPROEX SODIUM
Company:
WOCKHARDT
Original Approval or Tentative Approval Date:
June 5, 2006
Therapeutic Equivalents
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Approval History, Letters, Reviews and Related Documents
You can see the products in the same application. The table can be sorted by clicking the header columns.
Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
DIVALPROEX
DIVALPROEX SODIUM
125MG
TABLET, DELAYED RELEASE; ORAL
Tentative Approval
No
None
DIVALPROEX
DIVALPROEX SODIUM
250MG
TABLET, DELAYED RELEASE; ORAL
Tentative Approval
No
None
DIVALPROEX
DIVALPROEX SODIUM
500MG
TABLET, DELAYED RELEASE; ORAL
Tentative Approval
No
None
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