Quick answers
- What is Numbrino?
- Numbrino is a brand name of Cocaine hydrochloride, a prescription medicine. The FDA NDC Directory lists 1 Numbrino product in 1 strength and form.
- Who makes Numbrino?
- Omnivium Pharms holds the FDA application for Numbrino (NDA209575, approved January 10, 2020).
- Is there a generic or store brand of Numbrino?
- Yes. The FDA NDC Directory lists 3 other products with the same active ingredients, strength and form as a Numbrino product, 2 of them generic. Ask your pharmacist whether one is right for you.
- Has Numbrino been recalled?
- No recall linked to Numbrino products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Numbrino is
Each Numbrino 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.
Cocaine hydrochloride · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| cocaine hydrochloride 40 mg/mL solution (topical) | Numbrino | 3 products, 2 companies | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Cocaine hydrochloride →
FDA approval
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| NDA209575 | Omnivium Pharms | January 10, 2020 | 1 |
Companies that list Numbrino
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Numbrino products.
- Omnivium Pharmaceuticals LLC.1 product
Recalls
No recall linked to Numbrino 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.