# VARDENAFIL

NDC: 70710-1071
Generic name: VARDENAFIL
Labeler / Manufacturer: Zydus Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20181101

FDA application: ANDA208960

## Active ingredients

- VARDENAFIL HYDROCHLORIDE TRIHYDRATE: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70710-1071"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70710-1071
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5876e062-e604-42a7-99c3-5da30b8dac06