Product NDC: | 55154-5712 |
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 |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55154-5712 |
Labeler Name: | Cardinal Health |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA070799 |
Marketing Category: | ANDA |
Start Marketing Date: | 19870211 |
Package NDC: | 55154-5712-5 |
Package Description: | 5 VIAL, SINGLE-DOSE in 1 BAG (55154-5712-5) > 5 mL in 1 VIAL, SINGLE-DOSE |
NDC Code | 55154-5712-5 |
Proprietary Name | Dopamine Hydrochloride |
Package Description | 5 VIAL, SINGLE-DOSE in 1 BAG (55154-5712-5) > 5 mL in 1 VIAL, SINGLE-DOSE |
Product NDC | 55154-5712 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Dopamine Hydrochloride |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 19870211 |
Marketing Category Name | ANDA |
Labeler Name | Cardinal Health |
Substance Name | DOPAMINE HYDROCHLORIDE |
Strength Number | 40 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Catecholamine [EPC],Catecholamines [Chemical/Ingredient] |