Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Appco Pharma LLC | Piscataway, NJ, United States | Makes it, tests it, packages it, repackages it and relabels it | Problems found, fixed voluntarilyMay 14, 2026 · 9 inspections |
Product details
- Generic drug
- Lamivudine: every company that makes it
- Form
- tablet, oral
- Strength
- 300 mg
- Approval
- ANDA ANDA206974
- On the market since
- Feb 1, 2017
- Package NDCs
50742-624-60- Official label
- DailyMed (National Library of Medicine), updated Dec 24, 2018
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