# CLOBETASOL PROPIONATE

NDC: 59651-732
Generic name: CLOBETASOL PROPIONATE
Labeler / Manufacturer: Aurobindo Pharma Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: OINTMENT
Routes: TOPICAL
Marketing started: 20230928

FDA application: ANDA075057

## Active ingredients

- CLOBETASOL PROPIONATE: .5 mg/g

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"59651-732"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=59651-732
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e238bf90-f5fd-446d-9799-e8f8fed2f0a9