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Fluoxetine Hydrochloride - 0781-2822-01 - (Fluoxetine Hydrochloride)

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Drug Information of Fluoxetine Hydrochloride

Product NDC: 0781-2822
Proprietary Name: Fluoxetine Hydrochloride
Non Proprietary Name: Fluoxetine Hydrochloride
Active Ingredient(s): 20    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: 0781-2822
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075049
Marketing Category: ANDA
Start Marketing Date: 20020129

Package Information of Fluoxetine Hydrochloride

Package NDC: 0781-2822-01
Package Description: 100 CAPSULE in 1 BOTTLE (0781-2822-01)

NDC Information of Fluoxetine Hydrochloride

NDC Code 0781-2822-01
Proprietary Name Fluoxetine Hydrochloride
Package Description 100 CAPSULE in 1 BOTTLE (0781-2822-01)
Product NDC 0781-2822
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fluoxetine Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20020129
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name FLUOXETINE HYDROCHLORIDE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of Fluoxetine Hydrochloride


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