Quick answers
- What is BESREMi?
- BESREMi is a brand name of Ropeginterferon ALFA-2B, a prescription medicine. The FDA NDC Directory lists 1 BESREMi product in 1 strength and form.
- Who makes BESREMi?
- Pharmaessentia Corp holds the FDA application for BESREMi (BLA761166, approved November 12, 2021).
- Is there a generic or store brand of BESREMi?
- Other products of Ropeginterferon ALFA-2B are listed with the FDA, but none in exactly the same strength and form as a BESREMi product.
- Has BESREMi been recalled?
- No recall linked to BESREMi products (by their NDC code or label) appears in the FDA enforcement reports we use.
What BESREMi is
Each BESREMi 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.
Ropeginterferon ALFA-2B · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| ropeginterferon ALFA-2B 500 ug/mL injection (subcutaneous) | BESREMi | None listed | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Ropeginterferon ALFA-2B →
FDA approval
- BLA: Biologics License Application: how a biologic medicine (made from living cells) is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| BLA761166 | Pharmaessentia Corp | November 12, 2021 | 1 |
Companies that list BESREMi
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of BESREMi products.
- PharmaEssentia USA1 product
Recalls
No recall linked to BESREMi 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.