NDC 51407-666 – Acebutolol Hydrochloride

Acebutolol Hydrochloride 200 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC51407-666

Product details

Brand name
Acebutolol Hydrochloride
Generic name
Acebutolol Hydrochloride
Labeler
Golden State Medical Supply, Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA074007
Marketed since
October 18, 1995
Listing expires
December 31, 2026
Pharmacologic class
beta-Adrenergic Blocker

Active ingredients

Uses, dosage, side effects and warnings for Acebutolol Hydrochloride →

Package NDC codes (1)

Package NDCDescriptionSince
51407-666-01100 CAPSULE in 1 BOTTLE (51407-666-01)Aug 1, 2022

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