NDC 68788-8834 – Atenolol

Atenolol 50 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68788-8834

Product details

Brand name
Atenolol
Generic name
Atenolol
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA078512
Marketed since
February 21, 2025
Listing expires
December 31, 2026
Pharmacologic class
beta-Adrenergic Blocker

Active ingredients

Uses, dosage, side effects and warnings for Atenolol →

Package NDC codes (4)

Package NDCDescriptionSince
68788-8834-1100 TABLET in 1 BOTTLE (68788-8834-1)Feb 21, 2025
68788-8834-330 TABLET in 1 BOTTLE (68788-8834-3)Feb 21, 2025
68788-8834-660 TABLET in 1 BOTTLE (68788-8834-6)Feb 21, 2025
68788-8834-990 TABLET in 1 BOTTLE (68788-8834-9)Feb 21, 2025

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