Product NDC: | 49349-991 |
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: | 49349-991 |
Labeler Name: | REMEDYREPACK INC. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021519 |
Marketing Category: | NDA |
Start Marketing Date: | 20121015 |
Package NDC: | 49349-991-02 |
Package Description: | 30 TABLET in 1 BLISTER PACK (49349-991-02) |
NDC Code | 49349-991-02 |
Proprietary Name | FLuvoxamine Maleate |
Package Description | 30 TABLET in 1 BLISTER PACK (49349-991-02) |
Product NDC | 49349-991 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | FLUVOXAMINE MALEATE |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20121015 |
Marketing Category Name | NDA |
Labeler Name | REMEDYREPACK INC. |
Substance Name | FLUVOXAMINE MALEATE |
Strength Number | 50 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |