Product NDC: | 0409-7809 |
Proprietary Name: | Dopamine Hydrochloride and Dextrose |
Non Proprietary Name: | DOPAMINE HYDROCHLORIDE |
Active Ingredient(s): | 1.6 mg/mL & nbsp; DOPAMINE HYDROCHLORIDE |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0409-7809 |
Labeler Name: | Hospira, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA018826 |
Marketing Category: | NDA |
Start Marketing Date: | 19830930 |
Package NDC: | 0409-7809-24 |
Package Description: | 500 mL in 1 BAG (0409-7809-24) |
NDC Code | 0409-7809-24 |
Proprietary Name | Dopamine Hydrochloride and Dextrose |
Package Description | 500 mL in 1 BAG (0409-7809-24) |
Product NDC | 0409-7809 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | DOPAMINE HYDROCHLORIDE |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 19830930 |
Marketing Category Name | NDA |
Labeler Name | Hospira, Inc. |
Substance Name | DOPAMINE HYDROCHLORIDE |
Strength Number | 1.6 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Catecholamine [EPC],Catecholamines [Chemical/Ingredient] |