# Mupirocin

NDC: 68071-4321
Generic name: Mupirocin
Labeler / Manufacturer: NuCare Pharmaceuticals,Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: OINTMENT
Routes: TOPICAL
Marketing started: 20050923

FDA application: ANDA065170

## Active ingredients

- MUPIROCIN: 20 mg/g

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68071-4321"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68071-4321
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=66db1071-024f-aa19-e053-2a91aa0a8e39