# Tadalafil

NDC: 43598-574
Generic name: Tadalafil
Labeler / Manufacturer: Dr.Reddys Laboratories Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20190326

FDA application: ANDA210069

## Active ingredients

- TADALAFIL: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"43598-574"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43598-574
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=22b8a2e3-d1b8-f193-45fa-77cc62a1b941