Atenolol (Page 5 of 5)

HOW SUPPLIED

Atenolol Tablets USP:
Tablets of 50 mg atenolol, NDC 71205-229-30 (circular, biconvex, film coated white to offwhite tablets identified with “ATN” and “50” engraved on one side and lip like score engraved on the other side) are supplied in bottles of 30 tablets.

Tablets of 50 mg atenolol, NDC 71205-229-60 (circular, biconvex, film coated white to offwhite tablets identified with “ATN” and “50” engraved on one side and lip like score engraved on the other side) are supplied in bottles of 60 tablets.

Tablets of 50 mg atenolol, NDC 71205-229-90 (circular, biconvex, film coated white to offwhite tablets identified with “ATN” and “50” engraved on one side and lip like score engraved on the other side) are supplied in bottles of 90 tablets.

Dispense in a well-closed, light-resistant containers.


Manufactured by:
Unique Pharmaceutical Laboratories
(A Div. of J. B. Chemicals & Pharmaceuticals Ltd.)
Mumbai 400 030, India
Distributed by:
Rising Pharmaceuticals, Inc.
Saddle Brook, NJ 07663

Repackaged by:
Proficient Rx LP
Thousand Oaks, CA 91320

Jul. 1018

50 mg- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

50 mg- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 71205-229-30

Atenolol Tablets, USP

50 mg

30 Tablets

Rx only

71205-229-30
(click image for full-size original)
ATENOLOL atenolol tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:71205-229(NDC:64980-438)
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
MAGNESIUM STEARATE
MICROCRYSTALLINE CELLULOSE
POVIDONE, UNSPECIFIED
SODIUM STARCH GLYCOLATE TYPE A POTATO
HYPROMELLOSE, UNSPECIFIED
titanium dioxide
glycerin
Product Characteristics
Color WHITE Score 2 pieces
Shape ROUND Size 8mm
Flavor Imprint Code ATN;50
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:71205-229-30 30 TABLET in 1 BOTTLE None
2 NDC:71205-229-60 60 TABLET in 1 BOTTLE None
3 NDC:71205-229-90 90 TABLET in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA077443 06/10/2010
Labeler — Proficient Rx LP (079196022)
Establishment
Name Address ID/FEI Operations
Proficient Rx LP 079196022 REPACK (71205-229), RELABEL (71205-229)

Revised: 07/2022 Proficient Rx LP

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