# Podofilox

NDC: 0574-0621
Generic name: Podofilox
Labeler / Manufacturer: Padagis US LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: GEL
Routes: TOPICAL
Marketing started: 20231213

FDA application: ANDA211871

## Active ingredients

- PODOFILOX: 5 mg/g

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0574-0621"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0574-0621
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d2e70c5e-d4a9-4295-9eff-517ffb974e61