Atenolol

Product NDC

55700-531

11-digit product format

557000531

Labeler code

55700

Product ID

55700-531_5b338229-eae6-4e42-8200-1f9ab3f7996e

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Atenolol

Dosage form

TABLET

Route

ORAL

Labeler

Lake Erie Medical DBA Quality Care Products LLC

Application

ANDA076900

Marketing category

ANDA

Marketing start

2017-06-23

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

2020-12-31

Current FDA listing

Historical FDA.report record