# Betaxolol

NDC: 24658-701
Generic name: Betaxolol
Labeler / Manufacturer: PuraCap Laboratories LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20160822

FDA application: ANDA075541

## Active ingredients

- BETAXOLOL HYDROCHLORIDE: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"24658-701"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=24658-701
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e198244d-fda3-4015-8c01-390f3f88e238