NDC 68788-8739 – Atenolol

Atenolol 25 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68788-8739

Product details

Brand name
Atenolol
Generic name
Atenolol
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA213136
Marketed since
September 20, 2024
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
68788-8739-1100 TABLET in 1 BOTTLE (68788-8739-1)Sep 20, 2024
68788-8739-330 TABLET in 1 BOTTLE (68788-8739-3)Sep 20, 2024
68788-8739-660 TABLET in 1 BOTTLE (68788-8739-6)Sep 20, 2024
68788-8739-990 TABLET in 1 BOTTLE (68788-8739-9)Sep 20, 2024

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