Fluoxetine - 63739-494-40 - (Fluoxetine Capsules)

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Drug Information of Fluoxetine

Product NDC: 63739-494
Proprietary Name: Fluoxetine
Non Proprietary Name: Fluoxetine Capsules
Active Ingredient(s): 40    mg/1 & nbsp;   Fluoxetine Capsules
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Fluoxetine

Product NDC: 63739-494
Labeler Name: McKesson Packaging Services Business Unit of McKesson Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090223
Marketing Category: ANDA
Start Marketing Date: 20101118

Package Information of Fluoxetine

Package NDC: 63739-494-40
Package Description: 100 CAPSULE in 1 BOTTLE (63739-494-40)

NDC Information of Fluoxetine

NDC Code 63739-494-40
Proprietary Name Fluoxetine
Package Description 100 CAPSULE in 1 BOTTLE (63739-494-40)
Product NDC 63739-494
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fluoxetine Capsules
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20101118
Marketing Category Name ANDA
Labeler Name McKesson Packaging Services Business Unit of McKesson Corporation
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


General Information