fluoxetine - 0615-1357-31 - (fluoxetine hydrochloride)

Alphabetical Index


Drug Information of fluoxetine

Product NDC: 0615-1357
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: 0615-1357
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075245
Marketing Category: ANDA
Start Marketing Date: 20100429

Package Information of fluoxetine

Package NDC: 0615-1357-31
Package Description: 31 CAPSULE in 1 BLISTER PACK (0615-1357-31)

NDC Information of fluoxetine

NDC Code 0615-1357-31
Proprietary Name fluoxetine
Package Description 31 CAPSULE in 1 BLISTER PACK (0615-1357-31)
Product NDC 0615-1357
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name fluoxetine hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20100429
Marketing Category Name ANDA
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
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