Product NDC: | 0409-2304 |
Proprietary Name: | Corlopam |
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: | 0409-2304 |
Labeler Name: | Hospira, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA019922 |
Marketing Category: | NDA |
Start Marketing Date: | 19970923 |
Package NDC: | 0409-2304-02 |
Package Description: | 1 AMPULE in 1 BOX (0409-2304-02) > 2 mL in 1 AMPULE |
NDC Code | 0409-2304-02 |
Proprietary Name | Corlopam |
Package Description | 1 AMPULE in 1 BOX (0409-2304-02) > 2 mL in 1 AMPULE |
Product NDC | 0409-2304 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | FENOLDOPAM MESYLATE |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 19970923 |
Marketing Category Name | NDA |
Labeler Name | Hospira, Inc. |
Substance Name | FENOLDOPAM MESYLATE |
Strength Number | 10 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Dopamine Agonists [MoA],Dopaminergic Agonist [EPC] |