Active Ingredient: VALPROIC ACID
Proprietary Name: VALPROIC ACID
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 250MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A070195
Product Number: 001
Approval Date: Jul 2, 1987
Applicant Holder Full Name: RP SCHERER NORTH AMERICA DIV RP SCHERER CORP
Marketing Status:
Discontinued
Patent and Exclusivity Information
