Product NDC: | 60505-0164 |
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 |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 60505-0164 |
Labeler Name: | Apotex Corp |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA075902 |
Marketing Category: | ANDA |
Start Marketing Date: | 20010710 |
Package NDC: | 60505-0164-2 |
Package Description: | 1000 TABLET in 1 BOTTLE (60505-0164-2) |
NDC Code | 60505-0164-2 |
Proprietary Name | Fluvoxamine Maleate |
Package Description | 1000 TABLET in 1 BOTTLE (60505-0164-2) |
Product NDC | 60505-0164 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Fluvoxamine Maleate |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20010710 |
Marketing Category Name | ANDA |
Labeler Name | Apotex Corp |
Substance Name | FLUVOXAMINE MALEATE |
Strength Number | 25 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |