# Nebivolol

NDC: 72603-871
Generic name: Nebivolol
Labeler / Manufacturer: NorthStar RxLLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20250714

FDA application: ANDA212661

## Active ingredients

- NEBIVOLOL HYDROCHLORIDE: 5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72603-871"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72603-871
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9a81733f-abb2-4090-a1e1-cbca356821e8