Fluoxetine - 0093-6108-12 - (Fluoxetine)

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Drug Information of Fluoxetine

Product NDC: 0093-6108
Proprietary Name: Fluoxetine
Non Proprietary Name: Fluoxetine
Active Ingredient(s): 20    mg/5mL & nbsp;   Fluoxetine
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Fluoxetine

Product NDC: 0093-6108
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075506
Marketing Category: ANDA
Start Marketing Date: 20010802

Package Information of Fluoxetine

Package NDC: 0093-6108-12
Package Description: 120 mL in 1 BOTTLE (0093-6108-12)

NDC Information of Fluoxetine

NDC Code 0093-6108-12
Proprietary Name Fluoxetine
Package Description 120 mL in 1 BOTTLE (0093-6108-12)
Product NDC 0093-6108
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fluoxetine
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20010802
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name FLUOXETINE HYDROCHLORIDE
Strength Number 20
Strength Unit mg/5mL
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of Fluoxetine


General Information