Active Ingredient: VIGABATRIN
Proprietary Name: VIGABATRIN
Dosage Form; Route of Administration: FOR SOLUTION; ORAL
Strength: 500MG/PACKET
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A214671
Product Number: 001
Approval Date: Mar 2, 2023
Applicant Holder Full Name: ZYDUS LIFESCIENCES GLOBAL FZE
Marketing Status:
Discontinued
Patent and Exclusivity Information