Fluoxetine (Page 13 of 13)

Package/Label Display Panel

Fluoxetine Capsules, USP

20 mg

10 Capsules

Bag label
(click image for full-size original)
FLUOXETINE
fluoxetine capsule
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:55154-1341(NDC:0904-5785)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
FLUOXETINE HYDROCHLORIDE (FLUOXETINE) FLUOXETINE 20 mg
Inactive Ingredients
Ingredient Name Strength
AMMONIA
D&C YELLOW NO. 10
FD&C BLUE NO. 1
GELATIN, UNSPECIFIED
MAGNESIUM STEARATE
STARCH, CORN
PROPYLENE GLYCOL
SHELLAC
TITANIUM DIOXIDE
Product Characteristics
Color WHITE Score no score
Shape CAPSULE Size 16mm
Flavor Imprint Code PLIVA;648
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:55154-1341-0 10 BLISTER PACK in 1 BAG contains a BLISTER PACK
1 1 CAPSULE in 1 BLISTER PACK This package is contained within the BAG (55154-1341-0)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA076001 02/16/2007
Labeler — Cardinal Health 107, LLC (118546603)

Revised: 01/2023 Cardinal Health 107, LLC

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