Atenolol (Page 7 of 7)

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

Atenolol tablets, USP for oral administration, are supplied as:

50 mg: round, white, scored tablets debossed GG 263 on one side and plain on the reverse side, and supplied as:

NDC 63187-201-30 bottles of 30

NDC 63187-201-60 bottles of 60

NDC 63187-201-90 bottles of 90

Store at 20°-25°C (68°-77°F) (see USP Controlled Room Temperature).

Dispense in a tight, light-resistant container.

11-2012M

7249

Sandoz Inc.

Princeton, NJ 08540

Repackaged By:

Proficient Rx LP

Thousand Oaks, CA 91320

50 mg Label

NDC 63187-201-90

Atenolol

Tablets, USP

50 mg

Rx only

30 Tablets

63187-201-30
(click image for full-size original)
ATENOLOL atenolol tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:63187-201(NDC:0781-1506)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ATENOLOL (ATENOLOL) ATENOLOL 50 mg
Inactive Ingredients
Ingredient Name Strength
MICROCRYSTALLINE CELLULOSE
MAGNESIUM STEARATE
SILICON DIOXIDE
SODIUM STARCH GLYCOLATE TYPE A POTATO
Product Characteristics
Color WHITE Score 2 pieces
Shape ROUND Size 7mm
Flavor Imprint Code GG263
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:63187-201-30 30 TABLET in 1 BOTTLE None
2 NDC:63187-201-60 60 TABLET in 1 BOTTLE None
3 NDC:63187-201-90 90 TABLET in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA073025 09/17/1991
Labeler — Proficient Rx LP (079196022)
Establishment
Name Address ID/FEI Operations
Proficient Rx LP 079196022 REPACK (63187-201), RELABEL (63187-201)

Revised: 01/2021 Proficient Rx LP

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