Atenolol

Product NDC

68788-9048

11-digit product format

687889048

Labeler code

68788

Product ID

68788-9048_84462551-4f53-4616-a9ad-c8b26626643e

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Atenolol

Dosage form

TABLET

Route

ORAL

Labeler

Preferred Pharmaceuticals, Inc.

Application

ANDA077877

Marketing category

ANDA

Marketing start

2007-12-04

Marketing end

0000-00-00

Substance

ATENOLOL

Active strength

50 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