Product NDC: | 21695-651 |
Proprietary Name: | Savella |
Non Proprietary Name: | milnacipran hydrochloride |
Active Ingredient(s): | 50 mg/1 & nbsp; milnacipran hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 21695-651 |
Labeler Name: | Rebel Distributors Corp |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA022256 |
Marketing Category: | NDA |
Start Marketing Date: | 20090417 |
Package NDC: | 21695-651-60 |
Package Description: | 60 TABLET, FILM COATED in 1 BOTTLE (21695-651-60) |
NDC Code | 21695-651-60 |
Proprietary Name | Savella |
Package Description | 60 TABLET, FILM COATED in 1 BOTTLE (21695-651-60) |
Product NDC | 21695-651 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | milnacipran hydrochloride |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20090417 |
Marketing Category Name | NDA |
Labeler Name | Rebel Distributors Corp |
Substance Name | MILNACIPRAN HYDROCHLORIDE |
Strength Number | 50 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Norepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |