FLUOXETINE - 16590-100-30 - (FLUOXETINE HYDROCHLORIDE)

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Drug Information of FLUOXETINE

Product NDC: 16590-100
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: 16590-100
Labeler Name: STAT RX USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075245
Marketing Category: ANDA
Start Marketing Date: 20100429

Package Information of FLUOXETINE

Package NDC: 16590-100-30
Package Description: 30 CAPSULE in 1 BOTTLE (16590-100-30)

NDC Information of FLUOXETINE

NDC Code 16590-100-30
Proprietary Name FLUOXETINE
Package Description 30 CAPSULE in 1 BOTTLE (16590-100-30)
Product NDC 16590-100
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 STAT RX USA LLC
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