Atenolol

Product NDC

0781-5229

11-digit product format

007815229

Labeler code

0781

Product ID

0781-5229_14beac7f-849f-4b5c-8ec4-dbca0979bd08

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Atenolol

Dosage form

TABLET

Route

ORAL

Labeler

Sandoz Inc

Application

ANDA073026

Marketing category

ANDA

Marketing start

1991-09-17

Marketing end

0000-00-00

Substance

ATENOLOL

Active strength

100 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