# mupirocin

NDC: 17856-0112
Generic name: Mupirocin
Labeler / Manufacturer: ATLANTIC BIOLOGICALS CORP.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: OINTMENT
Routes: TOPICAL
Marketing started: 20091030

FDA application: ANDA065123

## 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:"17856-0112"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=17856-0112
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=da2f7d4e-82c6-4790-8eea-3a97e5b30734