Fluoxetine - 76365-0101-2 - (Fluoxetine hydrochloride)

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Drug Information of Fluoxetine

Product NDC: 76365-0101
Proprietary Name: Fluoxetine
Non Proprietary Name: Fluoxetine hydrochloride
Active Ingredient(s): 10    mg/1 & nbsp;   Fluoxetine hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Fluoxetine

Product NDC: 76365-0101
Labeler Name: Prodigy Health Supplier
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075464
Marketing Category: ANDA
Start Marketing Date: 20120601

Package Information of Fluoxetine

Package NDC: 76365-0101-2
Package Description: 100 CAPSULE in 1 BOTTLE (76365-0101-2)

NDC Information of Fluoxetine

NDC Code 76365-0101-2
Proprietary Name Fluoxetine
Package Description 100 CAPSULE in 1 BOTTLE (76365-0101-2)
Product NDC 76365-0101
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fluoxetine hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20120601
Marketing Category Name ANDA
Labeler Name Prodigy Health Supplier
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