Quick answers
- What is Mycostatin?
- Mycostatin is a brand name of Nystatin, a prescription medicine. The FDA NDC Directory lists 1 Mycostatin product in 1 strength and form.
- Who makes Mycostatin?
- Padagis US holds the FDA application for Mycostatin (ANDA062225, approved December 11, 1979).
- Is there a generic or store brand of Mycostatin?
- Yes. The FDA NDC Directory lists 25 other products with the same active ingredients, strength and form as a Mycostatin product, 25 of them generic. Ask your pharmacist whether one is right for you.
- Has Mycostatin been recalled?
- No recall linked to Mycostatin products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Mycostatin is
Each Mycostatin 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.
Nystatin · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| nystatin 100000 USP units/g cream (topical) | Mycostatin | 25 products, 12 companies | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Nystatin →
FDA approval
- ANDA: Abbreviated New Drug Application: how a generic version is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| ANDA062225 | Padagis US | December 11, 1979 | 1 |
Companies that list Mycostatin
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Mycostatin products.
- Direct_Rx1 product
Recalls
No recall linked to Mycostatin 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.