Active Ingredient: DIVALPROEX SODIUM
Proprietary Name: DIVALPROEX SODIUM
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: EQ 250MG VALPROIC ACID
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A078239
Product Number: 001
Approval Date: Feb 27, 2009
Applicant Holder Full Name: ZYDUS PHARMACEUTICALS USA INC
Marketing Status:
Prescription
Patent and Exclusivity Information