Active Ingredient: DIVALPROEX SODIUM
Proprietary Name: DIVALPROEX SODIUM
Dosage Form; Route of Administration: TABLET, DELAYED RELEASE; ORAL
Strength: EQ 500MG VALPROIC ACID
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A079080
Product Number: 001
Approval Date: Feb 25, 2011
Applicant Holder Full Name: ACTAVIS LABORATORIES FL INC
Marketing Status:
Discontinued
Patent and Exclusivity Information