# Tadalafil

NDC: 35561-256
Generic name: Tadalafil
Labeler / Manufacturer: Bostal LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20191129

FDA application: ANDA208824

## Active ingredients

- TADALAFIL: 10 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"35561-256"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=35561-256
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=78509a43-a907-4359-9022-f38c4f765880