NDC 68382-023 – Atenolol

Atenolol 50 mg/1 · Tablet · Oral

Human Prescription Drug 2 recalls

Product NDC68382-023

Product details

Brand name
Atenolol
Generic name
Atenolol
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA076900
Marketed since
October 8, 2005
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
68382-023-01100 TABLET in 1 BOTTLE (68382-023-01)Oct 8, 2005
68382-023-022000 TABLET in 1 BOTTLE (68382-023-02)Oct 8, 2005
68382-023-101000 TABLET in 1 BOTTLE (68382-023-10)Oct 8, 2005
68382-023-1690 TABLET in 1 BOTTLE (68382-023-16)Oct 8, 2005
68382-023-2410000 TABLET in 1 BOTTLE (68382-023-24)Oct 8, 2005
68382-023-405000 TABLET in 1 BOTTLE (68382-023-40)Oct 8, 2005

Recalls mentioning this NDC

Other Atenolol products