# tadalafil

NDC: 71821-009
Generic name: Tadalafil
Labeler / Manufacturer: VKT Pharma Private Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20211104

FDA application: ANDA215556

## Active ingredients

- TADALAFIL: 20 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71821-009"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71821-009
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b4d9851c-5c06-4532-bd82-16d92b60c28f