NDC 51655-736 – Atenolol

Atenolol 100 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC51655-736

Product details

Brand name
Atenolol
Generic name
Atenolol
Labeler
Northwind Health Company, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA073457
Marketed since
June 17, 2021
Listing expires
December 31, 2027
Pharmacologic class
beta-Adrenergic Blocker

Active ingredients

Uses, dosage, side effects and warnings for Atenolol →

Package NDC codes (2)

Package NDCDescriptionSince
51655-736-2690 TABLET in 1 BOTTLE, PLASTIC (51655-736-26)Jan 28, 2022
51655-736-5230 TABLET in 1 BOTTLE, PLASTIC (51655-736-52)Jun 17, 2021

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