Atenolol

Product NDC

0904-5392

11-digit product format

009045392

Labeler code

0904

Product ID

0904-5392_dc040fcb-feb5-4101-b9eb-7cc464111d05

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Atenolol

Dosage form

TABLET

Route

ORAL

Labeler

Major Pharmaceuticals

Application

ANDA074052

Marketing category

ANDA

Marketing start

1992-05-01

Marketing end

2019-05-31

Substance

ATENOLOL

Active strength

25 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record