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Fluvoxamine Maleate - 0615-7569-39 - (Fluvoxamine Maleate)

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Drug Information of Fluvoxamine Maleate

Product NDC: 0615-7569
Proprietary Name: Fluvoxamine Maleate
Non Proprietary Name: Fluvoxamine Maleate
Active Ingredient(s): 100    mg/1 & nbsp;   Fluvoxamine Maleate
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Fluvoxamine Maleate

Product NDC: 0615-7569
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075893
Marketing Category: ANDA
Start Marketing Date: 20100312

Package Information of Fluvoxamine Maleate

Package NDC: 0615-7569-39
Package Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-7569-39)

NDC Information of Fluvoxamine Maleate

NDC Code 0615-7569-39
Proprietary Name Fluvoxamine Maleate
Package Description 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-7569-39)
Product NDC 0615-7569
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fluvoxamine Maleate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20100312
Marketing Category Name ANDA
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
Substance Name FLUVOXAMINE MALEATE
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of Fluvoxamine Maleate


General Information