FLUOXETINE - 43063-197-30 - (fluoxetine hydrochloride)

Alphabetical Index


Drug Information of FLUOXETINE

Product NDC: 43063-197
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: 43063-197
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076922
Marketing Category: ANDA
Start Marketing Date: 20081208

Package Information of FLUOXETINE

Package NDC: 43063-197-30
Package Description: 30 CAPSULE in 1 BOTTLE, PLASTIC (43063-197-30)

NDC Information of FLUOXETINE

NDC Code 43063-197-30
Proprietary Name FLUOXETINE
Package Description 30 CAPSULE in 1 BOTTLE, PLASTIC (43063-197-30)
Product NDC 43063-197
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 PD-Rx Pharmaceuticals, Inc.
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