Product NDC: | 62559-159 |
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, COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 62559-159 |
Labeler Name: | ANIP Acquisition Company |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021519 |
Marketing Category: | NDA AUTHORIZED GENERIC |
Start Marketing Date: | 20110809 |
Package NDC: | 62559-159-01 |
Package Description: | 100 TABLET, COATED in 1 BOTTLE (62559-159-01) |
NDC Code | 62559-159-01 |
Proprietary Name | fluvoxamine maleate |
Package Description | 100 TABLET, COATED in 1 BOTTLE (62559-159-01) |
Product NDC | 62559-159 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Fluvoxamine maleate |
Dosage Form Name | TABLET, COATED |
Route Name | ORAL |
Start Marketing Date | 20110809 |
Marketing Category Name | NDA AUTHORIZED GENERIC |
Labeler Name | ANIP Acquisition Company |
Substance Name | FLUVOXAMINE MALEATE |
Strength Number | 50 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |