# tadalafil

NDC: 35573-461
Generic name: Tadalafil
Labeler / Manufacturer: Burel Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20230401

FDA application: ANDA215556

## 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:"35573-461"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=35573-461
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a2e7f393-5cfc-45e5-b87d-9e8abc8e4355