Active Ingredient: VALPROATE SODIUM
Proprietary Name: DEPACON
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 100MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N020593
Product Number: 001
Approval Date: Dec 30, 1996
Applicant Holder Full Name: ABBVIE INC
Marketing Status:
Discontinued
Patent and Exclusivity Information