FLUOXETINE - 23155-029-10 - (FLUOXETINE)

Alphabetical Index


Drug Information of FLUOXETINE

Product NDC: 23155-029
Proprietary Name: FLUOXETINE
Non Proprietary Name: FLUOXETINE
Active Ingredient(s): 20    mg/1 & nbsp;   FLUOXETINE
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of FLUOXETINE

Product NDC: 23155-029
Labeler Name: Heritage Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA201336
Marketing Category: ANDA
Start Marketing Date: 20120629

Package Information of FLUOXETINE

Package NDC: 23155-029-10
Package Description: 1000 CAPSULE in 1 BOTTLE (23155-029-10)

NDC Information of FLUOXETINE

NDC Code 23155-029-10
Proprietary Name FLUOXETINE
Package Description 1000 CAPSULE in 1 BOTTLE (23155-029-10)
Product NDC 23155-029
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name FLUOXETINE
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20120629
Marketing Category Name ANDA
Labeler Name Heritage Pharmaceuticals Inc.
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


General Information