Atenolol

Product NDC

68645-493

11-digit product format

686450493

Labeler code

68645

Product ID

68645-493_1923e1fb-0ff0-4338-8505-29a779982dca

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Atenolol

Dosage form

TABLET

Route

ORAL

Labeler

Legacy Pharmaceutical Packaging, LLC

Application

ANDA076900

Marketing category

ANDA

Marketing start

2005-10-08

Marketing end

2020-04-30

Substance

ATENOLOL

Active strength

50 mg/1

Pharmacologic classes

Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record