Atenolol (Page 6 of 6)

Cessation of Therapy in Patients with Angina Pectoris

If withdrawal of atenolol therapy is planned, it should be achieved gradually and patients should be carefully observed and advised to limit physical activity to a minimum.

HOW SUPPLIED

Product: 68151-2471

NDC: 68151-2471-1 1 TABLET in a BLISTER PACK

Manufactured by:

Cadila Healthcare Ltd.

India.

Distributed by:

Zydus Pharmaceuticals USA Inc.

Pennington, NJ 08534

Rev.: 02/13

Revision Date : 02/05/2013

ATENOLOL TABLET

Label ImageLabel Image
ATENOLOL atenolol tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:68151-2471(NDC:68382-024)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ATENOLOL (ATENOLOL) ATENOLOL 100 mg
Inactive Ingredients
Ingredient Name Strength
ANHYDROUS CITRIC ACID
CROSCARMELLOSE SODIUM
MAGNESIUM STEARATE
SILICON DIOXIDE
POVIDONE, UNSPECIFIED
MICROCRYSTALLINE CELLULOSE
Product Characteristics
Color WHITE (WHITE TO OFF- WHITE) Score no score
Shape ROUND (ROUND) Size 10mm
Flavor Imprint Code Z;67
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:68151-2471-1 1 TABLET in 1 BLISTER PACK None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA076900 10/08/2005
Labeler — Carilion Materials Management (079239644)
Establishment
Name Address ID/FEI Operations
Carilion Materials Management 079239644 REPACK (68151-2471)

Revised: 02/2018 Carilion Materials Management

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