Atenolol

Product NDC

66267-030

11-digit product format

662670030

Labeler code

66267

Product ID

66267-030_9cbe3ab2-1a26-56ff-e053-2a95a90a2cfd

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Atenolol

Dosage form

TABLET

Route

ORAL

Labeler

NuCare Pharmaceuticals, Inc.

Application

ANDA074052

Marketing category

ANDA

Marketing start

1992-05-01

Marketing end

0000-00-00

Substance

ATENOLOL

Active strength

25 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