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Fluoxetine Hydrochloride - 49349-518-02 - (Fluoxetine Hydrochloride)

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Drug Information of Fluoxetine Hydrochloride

Product NDC: 49349-518
Proprietary Name: Fluoxetine Hydrochloride
Non Proprietary Name: Fluoxetine Hydrochloride
Active Ingredient(s): 10    mg/1 & nbsp;   Fluoxetine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Fluoxetine Hydrochloride

Product NDC: 49349-518
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078619
Marketing Category: ANDA
Start Marketing Date: 20110920

Package Information of Fluoxetine Hydrochloride

Package NDC: 49349-518-02
Package Description: 30 CAPSULE in 1 BLISTER PACK (49349-518-02)

NDC Information of Fluoxetine Hydrochloride

NDC Code 49349-518-02
Proprietary Name Fluoxetine Hydrochloride
Package Description 30 CAPSULE in 1 BLISTER PACK (49349-518-02)
Product NDC 49349-518
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fluoxetine Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20110920
Marketing Category Name ANDA
Labeler Name REMEDYREPACK 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 Hydrochloride


General Information