NDC 50268-050 – Acebutolol Hydrochloride

Acebutolol Hydrochloride 200 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC50268-050

Product details

Brand name
Acebutolol Hydrochloride
Generic name
Acebutolol Hydrochloride
Labeler
AvPAK
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA075047
Marketed since
September 16, 2010
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
50268-050-1550 BLISTER PACK in 1 BOX (50268-050-15) / 1 CAPSULE in 1 BLISTER PACK (50268-050-11)Sep 16, 2010

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