Quick answers
- What is Hemangeol?
- Hemangeol is a brand name of Propranolol hydrochloride, a prescription medicine. The FDA NDC Directory lists 2 Hemangeol products in 1 strength and form.
- Who makes Hemangeol?
- Eton holds the FDA application for Hemangeol (NDA205410, approved March 14, 2014). 1 other company (repackagers or distributors) also list Hemangeol products.
- Is there a generic or store brand of Hemangeol?
- Other products of Propranolol hydrochloride are listed with the FDA, but none in exactly the same strength and form as a Hemangeol product.
- Has Hemangeol been recalled?
- No recall linked to Hemangeol products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Hemangeol is
Each Hemangeol 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.
Propranolol hydrochloride · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| propranolol hydrochloride 4.28 mg/mL solution (oral) | Hemangeol | None listed | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Propranolol hydrochloride →
FDA approval
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| NDA205410 | Eton | March 14, 2014 | 2 |
Companies that list Hemangeol
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Hemangeol products.
- Pierre Fabre Pharmaceuticals, Inc.1 product
- Eton Pharmaceuticals, Inc.1 product
Recalls
No recall linked to Hemangeol 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.