Quick answers
- What is Evomela?
- Evomela is a brand name of Melphalan HCL, a prescription medicine. The FDA NDC Directory lists 1 Evomela product in 1 strength and form.
- Who makes Evomela?
- Acrotech Biopharma holds the FDA application for Evomela (NDA207155, approved March 10, 2016).
- Is there a generic or store brand of Evomela?
- Other products of Melphalan HCL are listed with the FDA, but none in exactly the same strength and form as a Evomela product.
- Has Evomela been recalled?
- No recall linked to Evomela products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Evomela is
Each Evomela 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.
Melphalan HCL · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| melphalan hydrochloride 50 mg/10 mL injection, powder, lyophilized, for solution (intravenous) | Evomela | None listed | — |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Melphalan HCL →
FDA approval
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| NDA207155 | Acrotech Biopharma | March 10, 2016 | 1 |
Companies that list Evomela
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Evomela products.
- Acrotech Biopharma Inc1 product
Recalls
No recall linked to Evomela 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.