# Nebivolol

NDC: 67877-393
Generic name: Nebivolol
Labeler / Manufacturer: Ascend Laboratories, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20210916

FDA application: ANDA203828

## 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:"67877-393"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=67877-393
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=fecef8fc-b66b-4133-b66f-8d6b72750622