NDC 68180-603

Lamivudine 300 mg tablet, film coated

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
Lamivudine: every company that makes it
Form
tablet, film coated
Strength
300 mg
Approval
ANDA ANDA205217
On the market since
Mar 25, 2015
Package NDCs
68180-603-06
Official label
DailyMed (National Library of Medicine), updated Jan 3, 2024

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