# VARDENAFIL HYDROCHLORIDE

NDC: 62332-236
Generic name: VARDENAFIL HYDROCHLORIDE
Labeler / Manufacturer: Alembic Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20200805

FDA application: ANDA214031

## Active ingredients

- VARDENAFIL HYDROCHLORIDE: 2.5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"62332-236"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=62332-236
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d2dce236-257e-44b6-93a9-9f0280257c6a