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Dopamine Hydrochloride and Dextrose
Dopamine Hydrochloride and Dextrose - 0409-7808-22 - (DOPAMINE HYDROCHLORIDE)
Drug Information of Dopamine Hydrochloride and Dextrose
| Product NDC: | 0409-7808 |
| Proprietary Name: | Dopamine Hydrochloride and Dextrose |
| Non Proprietary Name: | DOPAMINE HYDROCHLORIDE |
| Active Ingredient(s): | .8 mg/mL & nbsp; DOPAMINE HYDROCHLORIDE |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dopamine Hydrochloride and Dextrose
| Product NDC: | 0409-7808 |
| Labeler Name: | Hospira, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018826 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19830930 |
Package Information of Dopamine Hydrochloride and Dextrose
| Package NDC: | 0409-7808-22 |
| Package Description: | 250 mL in 1 BAG (0409-7808-22) |
NDC Information of Dopamine Hydrochloride and Dextrose
| NDC Code | 0409-7808-22 |
| Proprietary Name | Dopamine Hydrochloride and Dextrose |
| Package Description | 250 mL in 1 BAG (0409-7808-22) |
| Product NDC | 0409-7808 |
| 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 | .8 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Catecholamine [EPC],Catecholamines [Chemical/Ingredient] |
