Fluoxetine - 0093-7188-10 - (Fluoxetine Hydrochloride)

Alphabetical Index


Drug Information of Fluoxetine

Product NDC: 0093-7188
Proprietary Name: Fluoxetine
Non Proprietary Name: Fluoxetine Hydrochloride
Active Ingredient(s): 10    mg/1 & nbsp;   Fluoxetine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Fluoxetine

Product NDC: 0093-7188
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075872
Marketing Category: ANDA
Start Marketing Date: 20020130

Package Information of Fluoxetine

Package NDC: 0093-7188-10
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE (0093-7188-10)

NDC Information of Fluoxetine

NDC Code 0093-7188-10
Proprietary Name Fluoxetine
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE (0093-7188-10)
Product NDC 0093-7188
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fluoxetine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20020130
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name FLUOXETINE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of Fluoxetine


General Information