Quick answers
- What is Eylea Hd?
- Eylea Hd is a brand name of Aflibercept, a prescription medicine. The FDA NDC Directory lists 2 Eylea Hd products in 1 strength and form.
- Who makes Eylea Hd?
- Regeneron Pharmaceuticals holds the FDA application for Eylea Hd (BLA761355, approved August 18, 2023).
- Is there a generic or store brand of Eylea Hd?
- Other products of Aflibercept are listed with the FDA, but none in exactly the same strength and form as a Eylea Hd product.
- Has Eylea Hd been recalled?
- No recall linked to Eylea Hd products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Eylea Hd is
Each Eylea Hd 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.
Aflibercept · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| aflibercept 8 mg/0.07 mL injection, solution (intravitreal) | Eylea Hd | None listed | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Aflibercept →
FDA approval
- BLA: Biologics License Application: how a biologic medicine (made from living cells) is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| BLA761355 | Regeneron Pharmaceuticals | August 18, 2023 | 2 |
Companies that list Eylea Hd
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Eylea Hd products.
- Regeneron Pharmaceuticals, Inc2 products
Recalls
No recall linked to Eylea Hd 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.