Atenolol

Product NDC

66267-031

11-digit product format

662670031

Labeler code

66267

Product ID

66267-031_9cbd0098-51e8-916b-e053-2a95a90acf00

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Atenolol

Dosage form

TABLET

Route

ORAL

Labeler

NuCare Pharmaceuticals, Inc.

Application

ANDA076900

Marketing category

ANDA

Marketing start

2005-10-08

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

2021-12-31

Current FDA listing

Historical FDA.report record