# BETAMETHASONE DIPROPIONATE

NDC: 35573-107
Generic name: BETAMETHASONE DIPROPIONATE
Labeler / Manufacturer: Burel Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: OINTMENT, AUGMENTED
Routes: TOPICAL
Marketing started: 20250115

FDA application: ANDA218289

## 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:"35573-107"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=35573-107
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c8bda9a8-4dec-4084-84e5-4b4623390bd8