ACTAVIS LABS UT INC: Generic drug approval for CLINDAMYCIN PHOSPHATE AND BENZOYL PEROXIDE
ACTAVIS LABS UT INC: Generic drug approval for CLINDAMYCIN PHOSPHATE AND BENZOYL PEROXIDE. Dated 90 days ago, it serves as a historical benchmark. Score 45/100. As of 2026-11-05, from openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration).
Data as of · Compiled by Zalwin from openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration)
Free preview: all 7 published fields of this record are shown below. Locked: 499 related FdaApprovalPulse records and the 4-column CSV export.
| Field | Value |
|---|---|
| Sponsor | ACTAVIS LABS UT INC |
| Product | CLINDAMYCIN PHOSPHATE AND BENZOYL PEROXIDE |
| Generic / ingredient | BENZOYL PEROXIDE, CLINDAMYCIN PHOSPHATE |
| Approval | Generic drug approval (ANDA) |
| Application | ANDA208757 |
| Decided | 2026-08-07 |
| Panel / class | GEL, TOPICAL |
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CSV columns: Sponsor · Product · Approval · Decided · official source URL
- Source agency: openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration)
- Record date: 2026-08-07
- Data refreshed: 2026-11-05
- Refunds on request within 14 days
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LIVE PUBLIC DATA Source: openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration) · Last refreshed: Thu, 05 Nov 2026 08:47:15 GMT
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45 / 100 Score
- A generic launch.
What is the FdaApprovalPulse record for ACTAVIS LABS UT INC?
The FDA approved CLINDAMYCIN PHOSPHATE AND BENZOYL PEROXIDE (ANDA208757) for ACTAVIS LABS UT INC on 2026-08-07: generic drug approval (ANDA).
How does ACTAVIS LABS UT INC compare to other FdaApprovalPulse records?
It is 90 days old; check the official source for later updates before acting.
ACTAVIS LABS UT INC vs. top 3 peers
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FdaApprovalPulse: Generic drug approval (ANDA)
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From openFDA (PMA and Drugs@FDA). openFDA can lag FDA decisions by days to weeks. Drug supplement types follow the FDA submission class (labeling and REMS, manufacturing/CMC, efficacy, other). Company and product level only. Verify on FDA databases before relying on an approval.