# Nebivolol Hydrochloride

NDC: 29300-377
Generic name: Nebivolol Hydrochloride
Labeler / Manufacturer: Unichem Pharmaceuticals (USA), Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20220404

FDA application: ANDA213830

## Active ingredients

- NEBIVOLOL HYDROCHLORIDE: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"29300-377"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=29300-377
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b1762bbb-b5be-48a7-8101-bb736f28845a