Fluoxetine - 16714-352-02 - (Fluoxetine Hydrochloride)

Alphabetical Index


Drug Information of Fluoxetine

Product NDC: 16714-352
Proprietary Name: Fluoxetine
Non Proprietary Name: Fluoxetine Hydrochloride
Active Ingredient(s): 20    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: 16714-352
Labeler Name: NorthStar RxLLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090223
Marketing Category: ANDA
Start Marketing Date: 20090701

Package Information of Fluoxetine

Package NDC: 16714-352-02
Package Description: 1000 CAPSULE in 1 BOTTLE (16714-352-02)

NDC Information of Fluoxetine

NDC Code 16714-352-02
Proprietary Name Fluoxetine
Package Description 1000 CAPSULE in 1 BOTTLE (16714-352-02)
Product NDC 16714-352
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fluoxetine Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20090701
Marketing Category Name ANDA
Labeler Name NorthStar RxLLC
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