Acebutolol Hydrochloride

Product NDC

42291-102

11-digit product format

422910102

Labeler code

42291

Product ID

42291-102_76caa413-1032-154e-e053-2991aa0ade1a

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Acebutolol Hydrochloride

Dosage form

CAPSULE

Route

ORAL

Labeler

AvKARE, Inc.

Application

ANDA075047

Marketing category

ANDA

Marketing start

2009-12-14

Marketing end

0000-00-00

Substance

ACEBUTOLOL HYDROCHLORIDE

Active strength

400 mg/1

Pharmacologic classes

Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record