Atenolol

Product NDC

68071-3190

11-digit product format

680713190

Labeler code

68071

Product ID

68071-3190_8761e694-5681-92f4-e053-2a95a90a890a

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

25 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