# Betamethasone Dipropionate

NDC: 0168-0267
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: LOTION, AUGMENTED
Routes: TOPICAL
Marketing started: 20070521

FDA application: ANDA077111

## Active ingredients

- BETAMETHASONE DIPROPIONATE: .5 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0168-0267"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0168-0267
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4f411e41-00dc-47cf-8517-3ff5876e1bf5