Atenolol

Product NDC

55700-567

11-digit product format

557000567

Labeler code

55700

Product ID

55700-567_4e9f7d39-8e57-40e6-a405-065e6f79feda

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Atenolol

Dosage form

TABLET

Route

ORAL

Labeler

Lake Erie Medical DBA Quality Care Procucts LLC

Application

ANDA076900

Marketing category

ANDA

Marketing start

2017-12-15

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

2020-12-31

Current FDA listing

Historical FDA.report record