# KETOCONAZOLE

NDC: 72789-052
Generic name: KETOCONAZOLE
Labeler / Manufacturer: PD-Rx Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20180626

FDA application: ANDA210457

## Active ingredients

- KETOCONAZOLE: 200 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72789-052"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72789-052
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f162e616-21b4-49b1-b437-15e21001a6f0