Fluoxetine - 0615-7625-39 - (Fluoxetine)

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Drug Information of Fluoxetine

Product NDC: 0615-7625
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: 0615-7625
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076001
Marketing Category: ANDA
Start Marketing Date: 20120320

Package Information of Fluoxetine

Package NDC: 0615-7625-39
Package Description: 30 CAPSULE in 1 BLISTER PACK (0615-7625-39)

NDC Information of Fluoxetine

NDC Code 0615-7625-39
Proprietary Name Fluoxetine
Package Description 30 CAPSULE in 1 BLISTER PACK (0615-7625-39)
Product NDC 0615-7625
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fluoxetine
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20120320
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