NDC 68180-521

Vigabatrin 500 mg powder, for solution

On the label: Lupin Pharmaceuticals, Inc..

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Lupin LimitedSalcette, IndiaMakes it and packages it Problems found, fixed voluntarilyNov 21, 2025 · 9 inspections, 1 with FDA action

Product details

Generic drug
Vigabatrin: every company that makes it
Form
powder, for solution
Strength
500 mg
Approval
ANDA ANDA211790
On the market since
Mar 10, 2022
Package NDCs
68180-521-50
Official label
DailyMed (National Library of Medicine), updated Dec 1, 2022

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