Product NDC: | 0338-1005 |
Proprietary Name: | Dopamine Hydrochloride and Dextrose |
Non Proprietary Name: | Dopamine Hydrochloride |
Active Ingredient(s): | 80 mg/100mL & nbsp; Dopamine Hydrochloride |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0338-1005 |
Labeler Name: | Baxter Healthcare Corporation |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA019615 |
Marketing Category: | NDA |
Start Marketing Date: | 20120125 |
Package NDC: | 0338-1005-03 |
Package Description: | 500 mL in 1 BAG (0338-1005-03) |
NDC Code | 0338-1005-03 |
Proprietary Name | Dopamine Hydrochloride and Dextrose |
Package Description | 500 mL in 1 BAG (0338-1005-03) |
Product NDC | 0338-1005 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Dopamine Hydrochloride |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20120125 |
Marketing Category Name | NDA |
Labeler Name | Baxter Healthcare Corporation |
Substance Name | DOPAMINE HYDROCHLORIDE |
Strength Number | 80 |
Strength Unit | mg/100mL |
Pharmaceutical Classes | Catecholamine [EPC],Catecholamines [Chemical/Ingredient] |