NDC 68788-4112 – Atenolol

Atenolol 100 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68788-4112

Product details

Brand name
Atenolol
Generic name
Atenolol
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA213136
Marketed since
April 22, 2026
Listing expires
December 31, 2027
Pharmacologic class
beta-Adrenergic Blocker

Active ingredients

Uses, dosage, side effects and warnings for Atenolol →

Package NDC codes (4)

Package NDCDescriptionSince
68788-4112-1100 TABLET in 1 BOTTLE (68788-4112-1)Apr 22, 2026
68788-4112-330 TABLET in 1 BOTTLE (68788-4112-3)Apr 22, 2026
68788-4112-660 TABLET in 1 BOTTLE (68788-4112-6)Apr 22, 2026
68788-4112-990 TABLET in 1 BOTTLE (68788-4112-9)Apr 22, 2026

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