FLUOXETINE - 63629-3312-2 - (fluoxetine hydrochloride)

Alphabetical Index


Drug Information of FLUOXETINE

Product NDC: 63629-3312
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: 63629-3312
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076922
Marketing Category: ANDA
Start Marketing Date: 20081208

Package Information of FLUOXETINE

Package NDC: 63629-3312-2
Package Description: 60 CAPSULE in 1 BOTTLE (63629-3312-2)

NDC Information of FLUOXETINE

NDC Code 63629-3312-2
Proprietary Name FLUOXETINE
Package Description 60 CAPSULE in 1 BOTTLE (63629-3312-2)
Product NDC 63629-3312
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name fluoxetine hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20081208
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
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