# Ketoconazole

NDC: 0093-3219
Generic name: Ketoconazole
Labeler / Manufacturer: Teva Pharmaceuticals USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CREAM
Routes: TOPICAL
Marketing started: 20190208

FDA application: ANDA075581

## Active ingredients

- KETOCONAZOLE: 20 mg/g

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0093-3219"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0093-3219
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7fc47a6a-3714-4598-ae3b-d5a229262c21