Active Ingredient: DIVALPROEX SODIUM
Proprietary Name: DEPAKOTE ER
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: EQ 250MG VALPROIC ACID
Reference Listed Drug: Yes
Reference Standard: No
TE Code: AB
Application Number: N021168
Product Number: 002
Approval Date: May 31, 2002
Applicant Holder Full Name: ABBVIE INC
Marketing Status:
Prescription
Patent and Exclusivity Information
