Quick answers
- What is Epivir?
- Epivir is a brand name of Lamivudine, a prescription medicine. The FDA NDC Directory lists 3 Epivir products in 3 strengths and forms.
- Who makes Epivir?
- Viiv Hlthcare holds the FDA application for Epivir (NDA020564, approved November 17, 1995).
- Is there a generic or store brand of Epivir?
- Yes. The FDA NDC Directory lists 20 other products with the same active ingredients, strength and form as a Epivir product, 20 of them generic. Ask your pharmacist whether one is right for you.
- Has Epivir been recalled?
- No recall linked to Epivir products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Epivir is
Each Epivir product as listed in the FDA NDC Directory, by active ingredient, strength and form, with its official label. “Same medicine, other names” counts the other products with exactly the same active ingredients, strength and form (generic versions, store brands and other brands); inactive ingredients can differ.
Lamivudine · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| lamivudine 10 mg/mL solution (oral) | Epivir | 4 products, 4 companies | — |
| lamivudine 150 mg tablet, film coated (oral) | Epivir | 10 products, 10 companies | — |
| lamivudine 300 mg tablet, film coated (oral) | Epivir | 6 products, 6 companies | — |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Lamivudine →
FDA approval
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
Companies that list Epivir
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Epivir products.
- ViiV Healthcare Company3 products
Recalls
No recall linked to Epivir products (by their NDC code or label) appears in the FDA enforcement reports.
Sources
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
- NADAC (National Average Drug Acquisition Cost) 2026 — Centers for Medicare & Medicaid Services (CMS), data.medicaid.gov, list of November 4, 2026, retrieved November 7, 2026
Which names get a brand page: a name the NDC Directory lists for a medicine, held by one company (the FDA application holder, or the company named on most of its products), that is not just a description, and that is not the only product of its medicine.