Active Ingredient: DIVALPROEX SODIUM
Proprietary Name: DEPAKOTE
Dosage Form; Route of Administration: CAPSULE, DELAYED REL PELLETS; ORAL
Strength: EQ 125MG VALPROIC ACID
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AB
Application Number: N019680
Product Number: 001
Approval Date: Sep 12, 1989
Applicant Holder Full Name: ABBVIE INC
Marketing Status:
Prescription
Patent and Exclusivity Information
