# Vardenafil

NDC: 33342-203
Generic name: Vardenafil
Labeler / Manufacturer: Macleods Pharmaceuticals Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20181026

FDA application: ANDA205988

## Active ingredients

- VARDENAFIL HYDROCHLORIDE TRIHYDRATE: 11.85 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"33342-203"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=33342-203
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0ad213e0-d18a-4e67-a405-df95322eaa52