NDC 71335-2531 – Atenolol

Atenolol 100 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2531

Product details

Brand name
Atenolol
Generic name
Atenolol
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA078512
Marketed since
October 31, 2007
Listing expires
December 31, 2026
Pharmacologic class
beta-Adrenergic Blocker

Active ingredients

Uses, dosage, side effects and warnings for Atenolol →

Package NDC codes (7)

Package NDCDescriptionSince
71335-2531-1100 TABLET in 1 BOTTLE (71335-2531-1)Nov 26, 2024
71335-2531-230 TABLET in 1 BOTTLE (71335-2531-2)Nov 26, 2024
71335-2531-360 TABLET in 1 BOTTLE (71335-2531-3)Nov 26, 2024
71335-2531-490 TABLET in 1 BOTTLE (71335-2531-4)Nov 26, 2024
71335-2531-520 TABLET in 1 BOTTLE (71335-2531-5)Nov 26, 2024
71335-2531-6180 TABLET in 1 BOTTLE (71335-2531-6)Nov 26, 2024
71335-2531-710 TABLET in 1 BOTTLE (71335-2531-7)Nov 26, 2024

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