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Fluoxetine Hydrochloride - 42291-279-90 - (fluoxetine hydrochloride)

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Drug Information of Fluoxetine Hydrochloride

Product NDC: 42291-279
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: 42291-279
Labeler Name: AvKARE, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075755
Marketing Category: ANDA
Start Marketing Date: 20120830

Package Information of Fluoxetine Hydrochloride

Package NDC: 42291-279-90
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE (42291-279-90)

NDC Information of Fluoxetine Hydrochloride

NDC Code 42291-279-90
Proprietary Name Fluoxetine Hydrochloride
Package Description 90 TABLET, FILM COATED in 1 BOTTLE (42291-279-90)
Product NDC 42291-279
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name fluoxetine hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120830
Marketing Category Name ANDA
Labeler Name AvKARE, 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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