Quick answers
- What is Symfi?
- Symfi is a brand name of Efavirenz, lamivudine and tenofovir disoproxil fumarate, a prescription medicine. The FDA NDC Directory lists 1 Symfi product in 1 strength and form.
- Who makes Symfi?
- Mylan Labs Ltd holds the FDA application for Symfi (NDA022142, approved March 22, 2018).
- Is there a generic or store brand of Symfi?
- Yes. The FDA NDC Directory lists 1 other product with the same active ingredients, strength and form as a Symfi product, 1 of them generic. Ask your pharmacist whether one is right for you.
- Has Symfi been recalled?
- No recall linked to Symfi products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Symfi is
Each Symfi 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.
Efavirenz, lamivudine and tenofovir disoproxil fumarate · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| efavirenz 600 mg · lamivudine 300 mg · tenofovir disoproxil fumarate 300 mg tablet, film coated (oral) | Symfi | 1 product, 1 company | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Efavirenz, lamivudine and tenofovir disoproxil fumarate →
FDA approval
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| NDA022142 | Mylan Labs Ltd | March 22, 2018 | 1 |
Companies that list Symfi
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Symfi products.
- Viatris Specialty LLC1 product
Recalls
No recall linked to Symfi 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.