Active Ingredient: VALPROATE SODIUM
Proprietary Name: VALPROATE SODIUM
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 100MG BASE/ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A208120
Product Number: 001
Approval Date: Dec 22, 2021
Applicant Holder Full Name: MYLAN PHARMACEUTICALS INC
Marketing Status:
Discontinued
Patent and Exclusivity Information