Atenolol

Product NDC

0781-5220

11-digit product format

007815220

Labeler code

0781

Product ID

0781-5220_14beac7f-849f-4b5c-8ec4-dbca0979bd08

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Atenolol

Dosage form

TABLET

Route

ORAL

Labeler

Sandoz Inc

Application

ANDA074052

Marketing category

ANDA

Marketing start

1992-05-01

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

2019-12-31

Current FDA listing

Historical FDA.report record