tine hydrochloride capsule
PRODUCT INFORMATION
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0002-3238
Route of Administration ORAL
ACTIVE INGREDIENT/ACTIVE MOIETY
Ingredient Name Basis of Strength Strength
Atomoxetine hydrochloride (UNII: 57WVB6I2W0) (Atomoxetine - UNII:ASW034S0B8) Atomoxetine 18 mg
INACTIVE INGREDIENTS
Ingredient Name Strength
STARCH, Corn (UNII: O8232NY3SJ)
DIMETHICONE (UNII: 92RU3N3Y1O)
Gelatin (UNII: 2G86QN327L)
sodium lauryl sulfate (UNII: 368GB5141J)
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
titanium dioxide (UNII: 15FIX9V2JP)
PRODUCT CHARACTERISTICS
Color white (opaque white) , yellow (gold) Score no score
Shape CAPSULE Size 16mm
Flavor Imprint Code LILLY;3238;18;mg
Contains
PACKAGING
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0002-3238-30 30 in 1 BOTTLE; Type 0: Not a Combination Product 01/10/2003
2 NDC:0002-3238-07 7 in 1 BOTTLE; Type 0: Not a Combination Product 01/10/2003
MARKETING INFORMATION
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA021411 11/26/2002
STRATTERA
atomoxetine hydrochloride capsule
PRODUCT INFORMATION
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0002-3228
Route of Administration ORAL
ACTIVE INGREDIENT/ACTIVE MOIETY
Ingredient Name Basis of Strength Strength
Atomoxetine hydrochloride (UNII: 57WVB6I2W0) (Atomoxetine - UNII:ASW034S0B8) Atomoxetine 25 mg
INACTIVE INGREDIENTS
Ingredient Name Strength
STARCH, Corn (UNII: O8232NY3SJ)
DIMETHICONE (UNII: 92RU3N3Y1O)
Gelatin (UNII: 2G86QN327L)
sodium lauryl sulfate (UNII: 368GB5141J)
FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
FERROSOFERRIC OXIDE (UNII: XM0M87F357)
titanium dioxide (UNII: 15FIX9V2JP)
PRODUCT CHARACTERISTICS
Color white (opaque white) , blue (opaque blue) Score no score
Shape CAPSULE Size 16mm
Flavor Imprint Code LILLY;3228;25;mg
Contains
PACKAGING
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0002-3228-30 30 in 1 BOTTLE; Type 0: Not a Combination Product 01/10/2003
2 NDC:0002-3228-07 7 in 1 BOTTLE; Type 0: Not a Combination Product 01/10/2003
MARKETING INFORMATION
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA021411 11/26/2002
STRATTERA
atomoxetine hydrochloride capsule
PRODUCT INFORMATION
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0002-3229
Route of Administration ORAL
ACTIVE INGREDIENT/ACTIVE MOIETY
Ingredient Name Basis of Strength Strength
Atomoxetine hydrochlorid |
