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Fluoxetine Hydrochloride - 67046-211-60 - (Fluoxetine Hydrochloride)

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Drug Information of Fluoxetine Hydrochloride

Product NDC: 67046-211
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): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Fluoxetine Hydrochloride

Product NDC: 67046-211
Labeler Name: Contract Pharmacy Services-PA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075245
Marketing Category: ANDA
Start Marketing Date: 20100405

Package Information of Fluoxetine Hydrochloride

Package NDC: 67046-211-60
Package Description: 60 CAPSULE in 1 BLISTER PACK (67046-211-60)

NDC Information of Fluoxetine Hydrochloride

NDC Code 67046-211-60
Proprietary Name Fluoxetine Hydrochloride
Package Description 60 CAPSULE in 1 BLISTER PACK (67046-211-60)
Product NDC 67046-211
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fluoxetine Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20100405
Marketing Category Name ANDA
Labeler Name Contract Pharmacy Services-PA
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


General Information