NDC 65162-669 – Acebutolol Hydrochloride

Acebutolol Hydrochloride 200 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC65162-669

Product details

Brand name
Acebutolol Hydrochloride
Generic name
Acebutolol Hydrochloride
Labeler
Amneal Pharmaceuticals LLC
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA075047
Marketed since
December 1, 2009
Listing expires
December 31, 2027
Pharmacologic class
beta-Adrenergic Blocker

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
65162-669-10100 CAPSULE in 1 BOTTLE (65162-669-10)Dec 1, 2009
65162-669-50500 CAPSULE in 1 BOTTLE (65162-669-50)Dec 1, 2009

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