Product NDC: | 0409-4142 |
Proprietary Name: | DOPamine Hydrochloride and Dextrose |
Non Proprietary Name: | Dopamine Hydrochloride |
Active Ingredient(s): | 160 mg/100mL & nbsp; Dopamine Hydrochloride |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0409-4142 |
Labeler Name: | Hospira, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA018132 |
Marketing Category: | NDA |
Start Marketing Date: | 20100628 |
Package NDC: | 0409-4142-02 |
Package Description: | 12 BOTTLE, GLASS in 1 CASE (0409-4142-02) > 250 mL in 1 BOTTLE, GLASS |
NDC Code | 0409-4142-02 |
Proprietary Name | DOPamine Hydrochloride and Dextrose |
Package Description | 12 BOTTLE, GLASS in 1 CASE (0409-4142-02) > 250 mL in 1 BOTTLE, GLASS |
Product NDC | 0409-4142 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Dopamine Hydrochloride |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20100628 |
Marketing Category Name | NDA |
Labeler Name | Hospira, Inc. |
Substance Name | DOPAMINE HYDROCHLORIDE |
Strength Number | 160 |
Strength Unit | mg/100mL |
Pharmaceutical Classes | Catecholamine [EPC],Catecholamines [Chemical/Ingredient] |