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: A090161
Product Number: 001
Approval Date: Mar 15, 2012
Applicant Holder Full Name: DR REDDYS LABORATORIES LTD
Marketing Status:
Prescription
Patent and Exclusivity Information
