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fluvoxamine maleate - 0185-0017-30 - (fluvoxamine maleate)

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Drug Information of fluvoxamine maleate

Product NDC: 0185-0017
Proprietary Name: fluvoxamine maleate
Non Proprietary Name: fluvoxamine maleate
Active Ingredient(s): 25    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: 0185-0017
Labeler Name: Eon Labs, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075888
Marketing Category: ANDA
Start Marketing Date: 20001129

Package Information of fluvoxamine maleate

Package NDC: 0185-0017-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (0185-0017-30)

NDC Information of fluvoxamine maleate

NDC Code 0185-0017-30
Proprietary Name fluvoxamine maleate
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (0185-0017-30)
Product NDC 0185-0017
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name fluvoxamine maleate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20001129
Marketing Category Name ANDA
Labeler Name Eon Labs, Inc.
Substance Name FLUVOXAMINE MALEATE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of fluvoxamine maleate


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