NDC Code(s) : 55289-653-30, 55289-653-90
Packager : PD-Rx Pharmaceuticals, Inc.

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

AtenololAtenolol TABLET
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:55289-653(NDC:63304-623)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ATENOLOL(UNII: 50VV3VW0TI)
(ATENOLOL - UNII:50VV3VW0TI) 		ATENOLOL100 mg
Inactive Ingredients
Ingredient Name Strength
MAGNESIUM CARBONATE(UNII: 0E53J927NA)
MAGNESIUM STEARATE(UNII: 70097M6I30)
SILICON DIOXIDE(UNII: ETJ7Z6XBU4)
SODIUM LAURYL SULFATE(UNII: 368GB5141J)
SODIUM STARCH GLYCOLATE TYPE A POTATO(UNII: 5856J3G2A2)
STARCH, CORN(UNII: O8232NY3SJ)
Product Characteristics
Color white Score no score
Shape ROUND Size 9 mm
Flavor Imprint Code RE;21
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:55289-653-3030 in 1 BOTTLE, PLASTIC Type 0: Not a Combination Product09/12/2011
2NDC:55289-653-9090 in 1 BOTTLE, PLASTIC Type 0: Not a Combination Product09/12/2011
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA077877 12/04/2007

PRINCIPAL DISPLAY PANEL

ATENOLOL Tablets, USP

100 mg

Rx Only

55289653 Label