# Betamethasone dipropionate

NDC: 51672-1390
Generic name: Betamethasone dipropionate
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SPRAY
Routes: TOPICAL
Marketing started: 20200617

FDA application: ANDA211722

## Active ingredients

- BETAMETHASONE DIPROPIONATE: .5 mg/g

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51672-1390"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51672-1390
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=dc3dd2f7-38ad-4c4c-8602-29b33cc6af90