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Fluoxetine Hydrochloride - 0615-5501-31 - (Fluoxetine)

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Drug Information of Fluoxetine Hydrochloride

Product NDC: 0615-5501
Proprietary Name: Fluoxetine Hydrochloride
Non Proprietary Name: Fluoxetine
Active Ingredient(s): 10    mg/1 & nbsp;   Fluoxetine
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Fluoxetine Hydrochloride

Product NDC: 0615-5501
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075755
Marketing Category: ANDA
Start Marketing Date: 20100113

Package Information of Fluoxetine Hydrochloride

Package NDC: 0615-5501-31
Package Description: 31 TABLET, FILM COATED in 1 BLISTER PACK (0615-5501-31)

NDC Information of Fluoxetine Hydrochloride

NDC Code 0615-5501-31
Proprietary Name Fluoxetine Hydrochloride
Package Description 31 TABLET, FILM COATED in 1 BLISTER PACK (0615-5501-31)
Product NDC 0615-5501
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fluoxetine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20100113
Marketing Category Name ANDA
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
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 Hydrochloride


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