# Acebutolol Hydrochloride

NDC: 51407-667
Generic name: Acebutolol Hydrochloride
Labeler / Manufacturer: Golden State Medical Supply, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 19951018

FDA application: ANDA074007

## Active ingredients

- ACEBUTOLOL HYDROCHLORIDE: 400 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51407-667"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51407-667
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f037a079-fde6-3588-e053-2995a90a6621