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DOPamine Hydrochloride
DOPamine Hydrochloride - 0409-5820-01 - (Dopamine Hydrochloride)
Drug Information of DOPamine Hydrochloride
| Product NDC: | 0409-5820 |
| Proprietary Name: | DOPamine Hydrochloride |
| Non Proprietary Name: | Dopamine Hydrochloride |
| Active Ingredient(s): | 40 mg/mL & nbsp; Dopamine Hydrochloride |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION, CONCENTRATE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DOPamine Hydrochloride
| Product NDC: | 0409-5820 |
| Labeler Name: | Hospira, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018132 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20110726 |
Package Information of DOPamine Hydrochloride
| Package NDC: | 0409-5820-01 |
| Package Description: | 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-5820-01) > 5 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of DOPamine Hydrochloride
| NDC Code | 0409-5820-01 |
| Proprietary Name | DOPamine Hydrochloride |
| Package Description | 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-5820-01) > 5 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 0409-5820 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Dopamine Hydrochloride |
| Dosage Form Name | INJECTION, SOLUTION, CONCENTRATE |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20110726 |
| Marketing Category Name | NDA |
| Labeler Name | Hospira, Inc. |
| Substance Name | DOPAMINE HYDROCHLORIDE |
| Strength Number | 40 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Catecholamine [EPC],Catecholamines [Chemical/Ingredient] |
