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FLUVOXAMINE MALEATE - 57664-361-13 - (fluvoxamine maleate)

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Drug Information of FLUVOXAMINE MALEATE

Product NDC: 57664-361
Proprietary Name: FLUVOXAMINE MALEATE
Non Proprietary Name: fluvoxamine maleate
Active Ingredient(s): 50    mg/1 & nbsp;   fluvoxamine maleate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of FLUVOXAMINE MALEATE

Product NDC: 57664-361
Labeler Name: Caraco Pharmaceutical Laboratories, Ltd.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075900
Marketing Category: ANDA
Start Marketing Date: 20060223

Package Information of FLUVOXAMINE MALEATE

Package NDC: 57664-361-13
Package Description: 500 TABLET in 1 BOTTLE (57664-361-13)

NDC Information of FLUVOXAMINE MALEATE

NDC Code 57664-361-13
Proprietary Name FLUVOXAMINE MALEATE
Package Description 500 TABLET in 1 BOTTLE (57664-361-13)
Product NDC 57664-361
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name fluvoxamine maleate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20060223
Marketing Category Name ANDA
Labeler Name Caraco Pharmaceutical Laboratories, Ltd.
Substance Name FLUVOXAMINE MALEATE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of FLUVOXAMINE MALEATE


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