# Mupirocin

NDC: 50268-568
Generic name: Mupirocin
Labeler / Manufacturer: AvPAK
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: OINTMENT
Routes: TOPICAL
Marketing started: 20190611

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:"50268-568"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50268-568
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8b10c706-ae9c-fc76-e053-2a95a90a4c73