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