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Fluoxetine Hydrochloride - 21695-321-00 - (fluoxetine hydrochloride)

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Drug Information of Fluoxetine Hydrochloride

Product NDC: 21695-321
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): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Fluoxetine Hydrochloride

Product NDC: 21695-321
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075755
Marketing Category: ANDA
Start Marketing Date: 20100113

Package Information of Fluoxetine Hydrochloride

Package NDC: 21695-321-00
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (21695-321-00)

NDC Information of Fluoxetine Hydrochloride

NDC Code 21695-321-00
Proprietary Name Fluoxetine Hydrochloride
Package Description 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (21695-321-00)
Product NDC 21695-321
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name fluoxetine hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20100113
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
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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