Quick answers
- What is Clotrimazole/Betameth?
- Clotrimazole/Betameth is a brand name of Clotrimazole and betamethasone dipropionate, a prescription medicine. The FDA NDC Directory lists 1 Clotrimazole/Betameth product in 1 strength and form.
- Who makes Clotrimazole/Betameth?
- Actavis Mid Atlantic holds the FDA application for Clotrimazole/Betameth (ANDA076002, approved August 2, 2002).
- Is there a generic or store brand of Clotrimazole/Betameth?
- Yes. The FDA NDC Directory lists 18 other products with the same active ingredients, strength and form as a Clotrimazole/Betameth product, 18 of them generic. Ask your pharmacist whether one is right for you.
- Has Clotrimazole/Betameth been recalled?
- No recall linked to Clotrimazole/Betameth products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Clotrimazole/Betameth is
Each Clotrimazole/Betameth 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.
Clotrimazole and betamethasone dipropionate · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| betamethasone dipropionate 0.05% · clotrimazole 1% cream (topical) | Clotrimazole/Betameth | 18 products, 14 companies | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Clotrimazole and betamethasone dipropionate →
FDA approval
- ANDA: Abbreviated New Drug Application: how a generic version is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| ANDA076002 | Actavis Mid Atlantic | August 2, 2002 | 1 |
Companies that list Clotrimazole/Betameth
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Clotrimazole/Betameth products.
- Direct_Rx1 product
Recalls
No recall linked to Clotrimazole/Betameth 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.