Fluoxetine - 67046-210-60 - (Fluoxetine)

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Drug Information of Fluoxetine

Product NDC: 67046-210
Proprietary Name: Fluoxetine
Non Proprietary Name: Fluoxetine
Active Ingredient(s): 10    mg/1 & nbsp;   Fluoxetine
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Fluoxetine

Product NDC: 67046-210
Labeler Name: Contract Pharmacy Services-PA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075452
Marketing Category: ANDA
Start Marketing Date: 20100730

Package Information of Fluoxetine

Package NDC: 67046-210-60
Package Description: 60 CAPSULE in 1 BLISTER PACK (67046-210-60)

NDC Information of Fluoxetine

NDC Code 67046-210-60
Proprietary Name Fluoxetine
Package Description 60 CAPSULE in 1 BLISTER PACK (67046-210-60)
Product NDC 67046-210
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fluoxetine
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20100730
Marketing Category Name ANDA
Labeler Name Contract Pharmacy Services-PA
Substance Name FLUOXETINE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of Fluoxetine


General Information