# Dapsone

NDC: 51672-1388
Generic name: Dapsone
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: GEL
Routes: TOPICAL
Marketing started: 20190626

FDA application: ANDA210191

## Active ingredients

- DAPSONE: 75 mg/g

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51672-1388"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51672-1388
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=32fcb7e0-5a6d-4d95-b81c-148012a54112