Quick answers
- What is Inderal La?
- Inderal La is a brand name of Propranolol hydrochloride, a prescription medicine. The FDA NDC Directory lists 4 Inderal La products in 4 strengths and forms.
- Who makes Inderal La?
- Ani Pharms holds the FDA application for Inderal La (NDA018553, approved April 19, 1983).
- Is there a generic or store brand of Inderal La?
- Yes. The FDA NDC Directory lists 59 other products with the same active ingredients, strength and form as a Inderal La product, 55 of them generic. Ask your pharmacist whether one is right for you.
- Has Inderal La been recalled?
- No recall linked to Inderal La products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Inderal La is
Each Inderal La 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 120 mg capsule, extended release (oral) | Inderal La | 15 products, 10 companies | DailyMed |
| propranolol hydrochloride 160 mg capsule, extended release (oral) | Inderal La | 9 products, 8 companies | DailyMed |
| propranolol hydrochloride 60 mg capsule, extended release (oral) | Inderal La | 18 products, 13 companies | DailyMed |
| propranolol hydrochloride 80 mg capsule, extended release (oral) | Inderal La | 17 products, 12 companies | 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 |
|---|---|---|---|
| NDA018553 | Ani Pharms | April 19, 1983 | 4 |
Companies that list Inderal La
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Inderal La products.
- ANI Pharmaceuticals, Inc.4 products
Recalls
No recall linked to Inderal La 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.