Atenolol

Product NDC

60760-059

11-digit product format

607600059

Labeler code

60760

Product ID

60760-059_790ef832-356d-f1c5-e053-2991aa0ae3ac

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Atenolol

Dosage form

TABLET

Route

ORAL

Labeler

St Marys Medical Park Pharmacy

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