NDC Code(s) : 49999-454-30
Packager : Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC

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:49999-454(NDC:63304-621)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ATENOLOL(UNII: 50VV3VW0TI)
(ATENOLOL - UNII:50VV3VW0TI) 		ATENOLOL25 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 6 mm
Flavor Imprint Code RE;19
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:49999-454-3030 in 1 BOTTLE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA077877 04/18/2012

PRINCIPAL DISPLAY PANEL

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