Fluoxetine - 51138-095-30 - (Fluoxetine Hydrochloride)

Alphabetical Index


Drug Information of Fluoxetine

Product NDC: 51138-095
Proprietary Name: Fluoxetine
Non Proprietary Name: Fluoxetine Hydrochloride
Active Ingredient(s): 40    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: 51138-095
Labeler Name: Med-Health Pharma, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078619
Marketing Category: ANDA
Start Marketing Date: 20110115

Package Information of Fluoxetine

Package NDC: 51138-095-30
Package Description: 30 CAPSULE in 1 BOTTLE (51138-095-30)

NDC Information of Fluoxetine

NDC Code 51138-095-30
Proprietary Name Fluoxetine
Package Description 30 CAPSULE in 1 BOTTLE (51138-095-30)
Product NDC 51138-095
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fluoxetine Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20110115
Marketing Category Name ANDA
Labeler Name Med-Health Pharma, LLC
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