Active Ingredient: DIVALPROEX SODIUM
Proprietary Name: DIVALPROEX SODIUM
Dosage Form; Route of Administration: CAPSULE, DELAYED REL PELLETS; ORAL
Strength: EQ 125MG VALPROIC ACID
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A213181
Product Number: 001
Approval Date: Mar 2, 2020
Applicant Holder Full Name: AJANTA PHARMA LTD
Marketing Status:
Prescription
Patent and Exclusivity Information
