Fluoxetine (Page 13 of 13)

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FLUOXETINE fluoxetine hydrochloride liquid
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:54838-523
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
FLUOXETINE HYDROCHLORIDE (FLUOXETINE) FLUOXETINE 20 mg in 5 mL
Inactive Ingredients
Ingredient Name Strength
ALCOHOL
BENZOIC ACID
GLYCERIN
SUCROSE
WATER
Product Characteristics
Color Score
Shape Size
Flavor SPEARMINT (flavor) Imprint Code
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:54838-523-40 120 mL in 1 BOTTLE, PLASTIC None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA077849 08/27/2009
Labeler — Lannett Company, Inc. (002277481)

Revised: 06/2021 Lannett Company, Inc.

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