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Dopamine Hydrochloride
Dopamine Hydrochloride - 52584-805-25 - (Dopamine Hydrochloride)
Drug Information of Dopamine Hydrochloride
| Product NDC: | 52584-805 |
| 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) |
Labeler Information of Dopamine Hydrochloride
| Product NDC: | 52584-805 |
| Labeler Name: | General Injectables & Vaccines, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA070799 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100701 |
Package Information of Dopamine Hydrochloride
| Package NDC: | 52584-805-25 |
| Package Description: | 1 VIAL, SINGLE-DOSE in 1 BAG (52584-805-25) > 5 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of Dopamine Hydrochloride
| NDC Code | 52584-805-25 |
| Proprietary Name | Dopamine Hydrochloride |
| Package Description | 1 VIAL, SINGLE-DOSE in 1 BAG (52584-805-25) > 5 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 52584-805 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Dopamine Hydrochloride |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20100701 |
| Marketing Category Name | ANDA |
| Labeler Name | General Injectables & Vaccines, Inc |
| Substance Name | DOPAMINE HYDROCHLORIDE |
| Strength Number | 40 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Catecholamine [EPC],Catecholamines [Chemical/Ingredient] |
