# NEBIVOLOL

NDC: 0904-7498
Generic name: nebivolol
Labeler / Manufacturer: Major Pharmaceuticals
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20250224

FDA application: ANDA212682

## Active ingredients

- NEBIVOLOL: 5 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0904-7498"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0904-7498
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3e9e1048-b5ea-4d6a-9363-3ee0d059e088