# Acebutolol Hydrochloride

NDC: 65162-670
Generic name: Acebutolol Hydrochloride
Labeler / Manufacturer: Amneal Pharmaceuticals LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20091201

FDA application: ANDA075047

## 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:"65162-670"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65162-670
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=28f8c26c-a1e1-4485-a45f-05c82f7a34b5