Drug
Who makes clindamycin phosphate and benzoyl peroxide?
12 companies list clindamycin phosphate and benzoyl peroxide as a human prescription drug, including under the names Acanya, ONEXTON, Neuac. Forms: gel; kit. Routes: topical.
Labellers from the openFDA NDC Directory. A labeller is the firm named on the label, not necessarily the site that made the product, and a listing is not an FDA approval. Data as of 24 Sept 2026. Methodology
Companies listing clindamycin phosphate and benzoyl peroxide
| Company | Forms | Application | NDCs | Registered sites |
|---|---|---|---|---|
| Sun Pharmaceutical Industries LimitedIndia | gel | ANDAANDA206218, ANDA206575, ANDA208683 | 3 | 13 |
| Bryant Ranch PrepackUnited States | gel | ANDAANDA209610, ANDA212433 | 3 | 1 |
| Encube Ethicals LimitedIndia | gel | ANDAANDA207194, ANDA212433 | 2 | 5 |
| Bausch Health US, LLCCanada | gel | NDANDA050819 | 2 | 1 |
| Oceanside Pharmaceuticals. | gel | NDA AUTHORIZED GENERICNDA050819 | 2 | 0 |
| Zydus Lifesciences LimitedIndia | gel | ANDAANDA210794 | 1 | 12 |
| Padagis Israel Pharmaceuticals LtdUnited States | gel | ANDAANDA209610 | 1 | 2 |
| Mayne Pharma International Pty Ltd.Australia | gel | ANDAANDA209610 | 1 | 1 |
| Zydus Pharmaceuticals USA Inc.India | gel | ANDAANDA210794 | 1 | 1 |
| Medimetriks Pharmaceuticals, Inc. | gel | ANDAANDA090979 | 1 | 0 |
| Mylan Pharmaceuticals, Inc. | kit | ANDAANDA065443 | 1 | 0 |
| Northstar Rx, LLC, | gel | ANDAANDA212433 | 1 | 0 |
Enquiry
Common questions
- Who makes clindamycin phosphate and benzoyl peroxide?
- 12 companies list clindamycin phosphate and benzoyl peroxide as a human prescription drug in the openFDA NDC Directory, led by Sun Pharmaceutical Industries Limited, Bryant Ranch Prepack, Encube Ethicals Limited, Bausch Health US, LLC, Oceanside Pharmaceuticals.. Each is the labeller, the firm named on the label; the product may be made at a site registered to another company.
- Is there a generic Acanya?
- 10 companies list clindamycin phosphate and benzoyl peroxide under an abbreviated new drug application (ANDA), the application type used for generics, and 1 under an NDA or BLA. Listing status is from the NDC Directory; it is not a statement of availability.