Atenolol

Product NDC

42291-142

11-digit product format

422910142

Labeler code

42291

Product ID

42291-142_62d7b3c5-cfaf-08d3-e053-2a91aa0abb8f

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Atenolol

Dosage form

TABLET

Route

ORAL

Labeler

AvKARE, Inc.

Application

ANDA074056

Marketing category

ANDA

Marketing start

2013-06-17

Marketing end

0000-00-00

Substance

ATENOLOL

Active strength

100 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record