Fluoxetine - 50111-647-02 - (Fluoxetine)

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Drug Information of Fluoxetine

Product NDC: 50111-647
Proprietary Name: Fluoxetine
Non Proprietary Name: Fluoxetine
Active Ingredient(s): 10    mg/1 & nbsp;   Fluoxetine
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Fluoxetine

Product NDC: 50111-647
Labeler Name: Pliva Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076001
Marketing Category: ANDA
Start Marketing Date: 20020129

Package Information of Fluoxetine

Package NDC: 50111-647-02
Package Description: 500 CAPSULE in 1 BOTTLE (50111-647-02)

NDC Information of Fluoxetine

NDC Code 50111-647-02
Proprietary Name Fluoxetine
Package Description 500 CAPSULE in 1 BOTTLE (50111-647-02)
Product NDC 50111-647
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fluoxetine
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20020129
Marketing Category Name ANDA
Labeler Name Pliva 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