Atomoxetine (Page 11 of 11)

Package/Label Display Panel

Atomoxetine Capsules, USP

40 mg

30 Capsules

Carton label
(click image for full-size original)
ATOMOXETINE
atomoxetine capsule
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0904-6908(NDC:55111-521)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Atomoxetine Hydrochloride (Atomoxetine) Atomoxetine 40 mg
Inactive Ingredients
Ingredient Name Strength
starch, corn
dimethicone
FD&C BLUE NO. 2
GELATIN, UNSPECIFIED
ferric oxide red
ferric oxide yellow
titanium dioxide
ferrosoferric oxide
butyl alcohol
alcohol
isopropyl alcohol
potassium hydroxide
propylene glycol
Shellac
ammonia
Product Characteristics
Color BLUE (dark blue) Score no score
Shape CAPSULE Size 19mm
Flavor Imprint Code RDY;521
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0904-6908-04 30 BLISTER PACK in 1 CARTON contains a BLISTER PACK
1 1 CAPSULE in 1 BLISTER PACK This package is contained within the CARTON (0904-6908-04)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA090609 02/23/2018
Labeler — Major Pharmaceuticals (191427277)

Revised: 07/2022 Major Pharmaceuticals

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