# Nebivolol

NDC: 72241-032
Generic name: Nebivolol
Labeler / Manufacturer: Modavar Pharmaceuticals LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20171229

FDA application: ANDA208717

## Active ingredients

- NEBIVOLOL HYDROCHLORIDE: 2.5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72241-032"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72241-032
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=19d20396-ade8-400e-94f4-69913637d051