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Fluoxetine Hydrochloride - 0781-2823-31 - (Fluoxetine Hydrochloride)

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Drug Information of Fluoxetine Hydrochloride

Product NDC: 0781-2823
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: 0781-2823
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075049
Marketing Category: ANDA
Start Marketing Date: 20010802

Package Information of Fluoxetine Hydrochloride

Package NDC: 0781-2823-31
Package Description: 30 CAPSULE in 1 BOTTLE (0781-2823-31)

NDC Information of Fluoxetine Hydrochloride

NDC Code 0781-2823-31
Proprietary Name Fluoxetine Hydrochloride
Package Description 30 CAPSULE in 1 BOTTLE (0781-2823-31)
Product NDC 0781-2823
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fluoxetine Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20010802
Marketing Category Name ANDA
Labeler Name Sandoz 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