# Clobetasol Propionate

NDC: 51672-1371
Generic name: Clobetasol Propionate
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SPRAY
Routes: TOPICAL
Marketing started: 20180326

FDA application: ANDA208842

## Active ingredients

- CLOBETASOL PROPIONATE: .05 g/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51672-1371"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51672-1371
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d8246614-757b-4e27-8c3e-37fcb401e6d9