# tadalafil

NDC: 71335-2583
Generic name: tadalafil
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20190326

FDA application: ANDA209250

## Active ingredients

- TADALAFIL: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71335-2583"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71335-2583
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=24b82a6a-1b7e-42e6-b29b-41d4ee4d525f