Quick answers
- What is Amphotericin B liposome?
- Amphotericin B liposome is a brand name of Amphotericin b, a prescription medicine. The FDA NDC Directory lists 1 Amphotericin B liposome product in 1 strength and form.
- Who makes Amphotericin B liposome?
- Mylan Labs Ltd holds the FDA application for Amphotericin B liposome (ANDA212967, approved June 30, 2025).
- Is there a generic or store brand of Amphotericin B liposome?
- Other products of Amphotericin b are listed with the FDA, but none in exactly the same strength and form as a Amphotericin B liposome product.
- Has Amphotericin B liposome been recalled?
- No recall linked to Amphotericin B liposome products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Amphotericin B liposome is
Each Amphotericin B liposome 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.
Amphotericin b · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| amphotericin b 50 mg/12.5 mL injection, powder, lyophilized, for suspension (intravenous) | Amphotericin B liposome | None listed | — |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Amphotericin b →
FDA approval
- ANDA: Abbreviated New Drug Application: how a generic version is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| ANDA212967 | Mylan Labs Ltd | June 30, 2025 | 1 |
Companies that list Amphotericin B liposome
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Amphotericin B liposome products.
- Mylan Institutional LLC1 product
Recalls
No recall linked to Amphotericin B liposome 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.