Quick answers
- What is Enoby?
- Enoby is a brand name of Denosumab, a prescription medicine. The FDA NDC Directory lists 1 Enoby product in 1 strength and form.
- Who makes Enoby?
- Hikma Pharmaceuticals USA Inc holds the FDA application for Enoby (BLA761439, approved September 26, 2025).
- Is there a generic or store brand of Enoby?
- Yes. The FDA NDC Directory lists 7 other products with the same active ingredients, strength and form as a Enoby product. Ask your pharmacist whether one is right for you.
- Has Enoby been recalled?
- No recall linked to Enoby products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Enoby is
Each Enoby 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.
Denosumab · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| denosumab 60 mg/mL injection (subcutaneous) | Enoby | 7 products, 6 companies | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Denosumab →
FDA approval
- BLA: Biologics License Application: how a biologic medicine (made from living cells) is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| BLA761439 | Hikma Pharmaceuticals USA Inc | September 26, 2025 | 1 |
Companies that list Enoby
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Enoby products.
- Hikma Pharmaceuticals USA Inc.1 product
Recalls
No recall linked to Enoby 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.