# Tadalafil

NDC: 60290-028
Generic name: Tadalafil
Labeler / Manufacturer: Umedica Laboratories USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20260215

FDA application: ANDA211298

## Active ingredients

- TADALAFIL: 5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"60290-028"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60290-028
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6caf3b55-9bf4-4355-9e25-8bf368943fdd