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Fluoxetine Hydrochloride - 54868-4562-1 - (fluoxetine)

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Drug Information of Fluoxetine Hydrochloride

Product NDC: 54868-4562
Proprietary Name: Fluoxetine Hydrochloride
Non Proprietary Name: fluoxetine
Active Ingredient(s): 40    mg/1 & nbsp;   fluoxetine
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Fluoxetine Hydrochloride

Product NDC: 54868-4562
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075207
Marketing Category: ANDA
Start Marketing Date: 20080725

Package Information of Fluoxetine Hydrochloride

Package NDC: 54868-4562-1
Package Description: 90 CAPSULE in 1 BOTTLE, PLASTIC (54868-4562-1)

NDC Information of Fluoxetine Hydrochloride

NDC Code 54868-4562-1
Proprietary Name Fluoxetine Hydrochloride
Package Description 90 CAPSULE in 1 BOTTLE, PLASTIC (54868-4562-1)
Product NDC 54868-4562
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name fluoxetine
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20080725
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name FLUOXETINE HYDROCHLORIDE
Strength Number 40
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of Fluoxetine Hydrochloride


General Information