Atenolol

Product NDC

53808-0900

11-digit product format

538080900

Labeler code

53808

Product ID

53808-0900_66c085b7-3ec3-43b4-a095-e04cf8d7a76a

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Atenolol

Dosage form

TABLET

Route

ORAL

Labeler

State of Florida DOH Central Pharmacy

Application

ANDA078512

Marketing category

ANDA

Marketing start

2009-07-01

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

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record