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Atenolol - Medication Information

Product NDC Code 65841-024
Drug Name

Atenolol

Type Generic
Pharm Class Adrenergic beta-Antagonists [MoA],
beta-Adrenergic Blocker [EPC]
Active Ingredients
Atenolol 100 mg/1
Route ORAL
Dosage Form TABLET
Application Number ANDA076900
Labeler Name Zydus Lifesciences Limited
Packages
Package NDC Code Description
65841-024-01 100 tablet in 1 bottle (65841-024-01)
65841-024-10 1000 tablet in 1 bottle (65841-024-10)
65841-024-16 90 tablet in 1 bottle (65841-024-16)
65841-024-40 5000 tablet in 1 bottle (65841-024-40)
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Spl product data elements

Usually a list of ingredients in a drug product.
Atenolol Atenolol ATENOLOL ATENOLOL ANHYDROUS CITRIC ACID CROSCARMELLOSE SODIUM MAGNESIUM STEARATE SILICON DIOXIDE POVIDONE CELLULOSE, MICROCRYSTALLINE WHITE TO OFF- WHITE ROUND Z;65 Atenolol Atenolol ATENOLOL ATENOLOL ANHYDROUS CITRIC ACID CROSCARMELLOSE SODIUM MAGNESIUM STEARATE SILICON DIOXIDE POVIDONE CELLULOSE, MICROCRYSTALLINE WHITE TO OFF- WHITE ROUND Z;66 Atenolol Atenolol ATENOLOL ATENOLOL ANHYDROUS CITRIC ACID CROSCARMELLOSE SODIUM MAGNESIUM STEARATE SILICON DIOXIDE POVIDONE CELLULOSE, MICROCRYSTALLINE WHITE TO OFF- WHITE ROUND Z;67

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL NDC 65841-022-01 in bottles of 100 tablets Atenolol Tablets USP, 25 mg R x only 100 Tablets NDC 65841-023-01 in bottles of 100 tablets Atenolol Tablets USP, 50 mg R x only 100 Tablets NDC 65841-024-01 in bottles of 100 tablets Atenolol Tablets USP, 100 mg R x only 100 Tablets Atenolol Tablets, 25 mg Atenolol Tablets, 50 mg Atenolol Tablets, 100 mg

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API