NDC 71335-1616 – Atenolol

Atenolol 25 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-1616

Product details

Brand name
Atenolol
Generic name
Atenolol
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA074056
Marketed since
November 16, 2004
Listing expires
December 31, 2026
Pharmacologic class
beta-Adrenergic Blocker

Active ingredients

Uses, dosage, side effects and warnings for Atenolol →

Package NDC codes (6)

Package NDCDescriptionSince
71335-1616-130 TABLET in 1 BOTTLE (71335-1616-1)Nov 16, 2004
71335-1616-2100 TABLET in 1 BOTTLE (71335-1616-2)Nov 16, 2004
71335-1616-360 TABLET in 1 BOTTLE (71335-1616-3)Nov 16, 2004
71335-1616-490 TABLET in 1 BOTTLE (71335-1616-4)Nov 16, 2004
71335-1616-520 TABLET in 1 BOTTLE (71335-1616-5)Nov 16, 2004
71335-1616-6180 TABLET in 1 BOTTLE (71335-1616-6)Nov 16, 2004

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