Atenolol

Product NDC

70518-1071

11-digit product format

705181071

Labeler code

70518

Product ID

70518-1071_9010dbba-ad92-a0f0-e053-2a95a90a6dd1

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

atenolol

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA073457

Marketing category

ANDA

Marketing start

2018-03-19

Marketing end

0000-00-00

Substance

ATENOLOL

Active strength

25 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