Atenolol

Product NDC

50090-3071

11-digit product format

500903071

Labeler code

50090

Product ID

50090-3071_0d066992-6769-4700-914c-f1eb3de13ec9

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Atenolol

Dosage form

TABLET

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA074056

Marketing category

ANDA

Marketing start

1995-02-22

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