# Clindamycin Phosphate and Benzoyl Peroxide

NDC: 51672-1381
Generic name: Clindamycin and Benzoyl Peroxide Gel
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: KIT
Routes: —
Marketing started: 20200121

FDA application: ANDA208776

## Active ingredients

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## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51672-1381"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51672-1381
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=bde03712-b9c7-4953-af2e-d3270ba1a917