Product NDC: | 42769-1225 |
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) |
Product NDC: | 42769-1225 |
Labeler Name: | BayPharma, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021519 |
Marketing Category: | NDA |
Start Marketing Date: | 20080125 |
Package NDC: | 42769-1225-0 |
Package Description: | 100 TABLET in 1 BOTTLE (42769-1225-0) |
NDC Code | 42769-1225-0 |
Proprietary Name | Fluvoxamine Maleate |
Package Description | 100 TABLET in 1 BOTTLE (42769-1225-0) |
Product NDC | 42769-1225 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Fluvoxamine Maleate |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20080125 |
Marketing Category Name | NDA |
Labeler Name | BayPharma, Inc. |
Substance Name | FLUVOXAMINE MALEATE |
Strength Number | 50 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |