Active Ingredient: DIVALPROEX SODIUM
Proprietary Name: DIVALPROEX SODIUM
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: EQ 500MG VALPROIC ACID
Reference Listed Drug: No
Reference Standard: Yes
TE Code: AB
Application Number: A203730
Product Number: 002
Approval Date: May 29, 2015
Applicant Holder Full Name: AMNEAL PHARMACEUTICALS
Marketing Status:
Prescription
Patent and Exclusivity Information