Quick answers
- What is Polycin?
- Polycin is a brand name of Bacitracin zinc and polymyxin b sulfate, a prescription medicine. The FDA NDC Directory lists 1 Polycin product in 1 strength and form.
- Who makes Polycin?
- Padagis US holds the FDA application for Polycin (ANDA065022, approved February 27, 2002).
- Is there a generic or store brand of Polycin?
- Yes. The FDA NDC Directory lists 4 other products with the same active ingredients, strength and form as a Polycin product, 4 of them generic. Ask your pharmacist whether one is right for you.
- Has Polycin been recalled?
- No recall linked to Polycin products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Polycin is
Each Polycin 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.
Bacitracin zinc and polymyxin b sulfate · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| bacitracin zinc 500 USP units/g · polymyxin b sulfate 10000 USP units/g ointment (ophthalmic) | Polycin | 4 products, 3 companies | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Bacitracin zinc and polymyxin b sulfate →
FDA approval
- ANDA: Abbreviated New Drug Application: how a generic version is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| ANDA065022 | Padagis US | February 27, 2002 | 1 |
Companies that list Polycin
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Polycin products.
- NuCare Pharmaceuticals, Inc.1 product
Recalls
No recall linked to Polycin 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.