Quick answers
- What is Neuac?
- Neuac is a brand name of Clindamycin phosphate and benzoyl peroxide, a prescription medicine. The FDA NDC Directory lists 1 Neuac product in 1 strength and form.
- Who makes Neuac?
- Padagis Israel holds the FDA application for Neuac (ANDA090979, approved June 26, 2012).
- Is there a generic or store brand of Neuac?
- Yes. The FDA NDC Directory lists 12 other products with the same active ingredients, strength and form as a Neuac product, 12 of them generic. Ask your pharmacist whether one is right for you.
- Has Neuac been recalled?
- No recall linked to Neuac products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Neuac is
Each Neuac 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.
Clindamycin phosphate and benzoyl peroxide · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| benzoyl peroxide 5% · clindamycin phosphate 1% gel (topical) | Neuac | 12 products, 9 companies | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Clindamycin phosphate and benzoyl peroxide →
FDA approval
- ANDA: Abbreviated New Drug Application: how a generic version is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| ANDA090979 | Padagis Israel | June 26, 2012 | 1 |
Companies that list Neuac
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Neuac products.
- Medimetriks Pharmaceuticals1 product
Recalls
No recall linked to Neuac 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.