NDC 0409-2346
Dobutamine in Dextrose
Dobutamine In Dextrose
Dobutamine in Dextrose is a Intravenous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Hospira, Inc.. The primary component is Dobutamine Hydrochloride.
Product ID | 0409-2346_03a39c90-e78b-4864-8d4c-b11ea1af9fc5 |
NDC | 0409-2346 |
Product Type | Human Prescription Drug |
Proprietary Name | Dobutamine in Dextrose |
Generic Name | Dobutamine In Dextrose |
Dosage Form | Injection, Solution |
Route of Administration | INTRAVENOUS |
Marketing Start Date | 2005-08-12 |
Marketing Category | NDA / NDA |
Application Number | NDA020201 |
Labeler Name | Hospira, Inc. |
Substance Name | DOBUTAMINE HYDROCHLORIDE |
Active Ingredient Strength | 100 mg/100mL |
Pharm Classes | Adrenergic beta-Agonists [MoA],beta-Adrenergic Agonist [EPC] |
NDC Exclude Flag | N |
Listing Certified Through | 2022-12-31 |