Atenolol

Product NDC

58118-2022

11-digit product format

581182022

Labeler code

58118

Product ID

58118-2022_7975635b-8bed-6f03-e053-2991aa0a1bf0

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Atenolol

Dosage form

TABLET

Route

ORAL

Labeler

Clinical Solutions Wholes

Application

ANDA076900

Marketing category

ANDA

Marketing start

2017-08-11

Marketing end

2019-04-01

Substance

ATENOLOL

Active strength

25 mg/1

Pharmacologic classes

Adrenergic beta

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record