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DOBUTAMINE HYDROCHLORIDE
DOBUTAMINE HYDROCHLORIDE - 0409-2344-88 - (DOBUTAMINE HYDROCHLORIDE)
Drug Information of DOBUTAMINE HYDROCHLORIDE
| Product NDC: | 0409-2344 |
| Proprietary Name: | DOBUTAMINE HYDROCHLORIDE |
| Non Proprietary Name: | DOBUTAMINE HYDROCHLORIDE |
| Active Ingredient(s): | 12.5 mg/mL & nbsp; DOBUTAMINE HYDROCHLORIDE |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION, CONCENTRATE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DOBUTAMINE HYDROCHLORIDE
| Product NDC: | 0409-2344 |
| Labeler Name: | Hospira, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074086 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110625 |
Package Information of DOBUTAMINE HYDROCHLORIDE
| Package NDC: | 0409-2344-88 |
| Package Description: | 10 VIAL, SINGLE-DOSE in 1 TRAY (0409-2344-88) > 20 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of DOBUTAMINE HYDROCHLORIDE
| NDC Code | 0409-2344-88 |
| Proprietary Name | DOBUTAMINE HYDROCHLORIDE |
| Package Description | 10 VIAL, SINGLE-DOSE in 1 TRAY (0409-2344-88) > 20 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 0409-2344 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | DOBUTAMINE HYDROCHLORIDE |
| Dosage Form Name | INJECTION, SOLUTION, CONCENTRATE |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20110625 |
| Marketing Category Name | ANDA |
| Labeler Name | Hospira, Inc. |
| Substance Name | DOBUTAMINE HYDROCHLORIDE |
| Strength Number | 12.5 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Adrenergic beta-Agonists [MoA],beta-Adrenergic Agonist [EPC] |
