# Betamethasone Dipropionate

NDC: 0168-0268
Generic name: betamethasone dipropionate
Labeler / Manufacturer: E. Fougera & Co. a division of Fougera Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: OINTMENT, AUGMENTED
Routes: TOPICAL
Marketing started: 19990622

FDA application: ANDA075373

## 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:"0168-0268"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0168-0268
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=853399f8-95a7-41f3-80e7-7ed8e3ff1a5e