Product NDC: | 0781-3005 |
Proprietary Name: | Fenoldopam Mesylate |
Non Proprietary Name: | Fenoldopam Mesylate |
Active Ingredient(s): | 10 mg/mL & nbsp; Fenoldopam Mesylate |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0781-3005 |
Labeler Name: | Sandoz Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA077155 |
Marketing Category: | ANDA |
Start Marketing Date: | 20050215 |
Package NDC: | 0781-3005-92 |
Package Description: | 1 AMPULE in 1 CARTON (0781-3005-92) > 2 mL in 1 AMPULE |
NDC Code | 0781-3005-92 |
Proprietary Name | Fenoldopam Mesylate |
Package Description | 1 AMPULE in 1 CARTON (0781-3005-92) > 2 mL in 1 AMPULE |
Product NDC | 0781-3005 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Fenoldopam Mesylate |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20050215 |
Marketing Category Name | ANDA |
Labeler Name | Sandoz Inc |
Substance Name | FENOLDOPAM MESYLATE |
Strength Number | 10 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Dopamine Agonists [MoA],Dopaminergic Agonist [EPC] |