NDC 70377-089

Vigabatrin 500 mg per 10 mL powder, for solution

On the label: Biocon Pharma Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Wes Pharma IncWestminster, MD, United StatesMakes it Problems found, fixed voluntarilyNov 20, 2025 · 7 inspections

Product details

Generic drug
Vigabatrin: every company that makes it
Form
powder, for solution
Strength
500 mg per 10 mL
Approval
ANDA ANDA213390
On the market since
Aug 29, 2022
Package NDCs
70377-089-01
Official label
DailyMed (National Library of Medicine), updated Nov 10, 2022

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