Product NDC: | 47335-232 |
Proprietary Name: | Rizatriptan Benzoate |
Non Proprietary Name: | Rizatriptan Benzoate |
Active Ingredient(s): | 10 mg/1 & nbsp; Rizatriptan Benzoate |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 47335-232 |
Labeler Name: | Sun Pharma Global FZE |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA202047 |
Marketing Category: | ANDA |
Start Marketing Date: | 20130112 |
Package NDC: | 47335-232-88 |
Package Description: | 100 TABLET in 1 BOTTLE (47335-232-88) |
NDC Code | 47335-232-88 |
Proprietary Name | Rizatriptan Benzoate |
Package Description | 100 TABLET in 1 BOTTLE (47335-232-88) |
Product NDC | 47335-232 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Rizatriptan Benzoate |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20130112 |
Marketing Category Name | ANDA |
Labeler Name | Sun Pharma Global FZE |
Substance Name | RIZATRIPTAN BENZOATE |
Strength Number | 10 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Serotonin 1b Receptor Agonists [MoA],Serotonin 1d Receptor Agonists [MoA],Serotonin-1b and Serotonin-1d Receptor Agonist [EPC] |