# Calcipotriene and Betamethasone Dipropionate

NDC: 51672-1402
Generic name: Calcipotriene and Betamethasone Dipropionate
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SUSPENSION
Routes: TOPICAL
Marketing started: 20200902

FDA application: ANDA213269

## Active ingredients

- BETAMETHASONE DIPROPIONATE: 50 mg/g
- CALCIPOTRIENE: 50 ug/g

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51672-1402"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51672-1402
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1d0ab2e6-1ab1-4d3e-ad55-7fa26446f191