| Product NDC: | 0409-7810 |
| Proprietary Name: | Dopamine Hydrochloride and Dextrose |
| Non Proprietary Name: | DOPAMINE HYDROCHLORIDE |
| Active Ingredient(s): | 3.2 mg/mL & nbsp; DOPAMINE HYDROCHLORIDE |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0409-7810 |
| Labeler Name: | Hospira, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018826 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19830930 |
| Package NDC: | 0409-7810-22 |
| Package Description: | 250 mL in 1 BAG (0409-7810-22) |
| NDC Code | 0409-7810-22 |
| Proprietary Name | Dopamine Hydrochloride and Dextrose |
| Package Description | 250 mL in 1 BAG (0409-7810-22) |
| Product NDC | 0409-7810 |
| 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 | 3.2 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Catecholamine [EPC],Catecholamines [Chemical/Ingredient] |