Product NDC: | 54868-5777 |
Proprietary Name: | Dobutamine Hydrochloride |
Non Proprietary Name: | Dobutamine Hydrochloride |
Active Ingredient(s): | 400 mg/100mL & nbsp; Dobutamine Hydrochloride |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54868-5777 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020201 |
Marketing Category: | NDA |
Start Marketing Date: | 20070613 |
Package NDC: | 54868-5777-0 |
Package Description: | 12 BAG in 1 CASE (54868-5777-0) > 250 mL in 1 BAG |
NDC Code | 54868-5777-0 |
Proprietary Name | Dobutamine Hydrochloride |
Package Description | 12 BAG in 1 CASE (54868-5777-0) > 250 mL in 1 BAG |
Product NDC | 54868-5777 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Dobutamine Hydrochloride |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20070613 |
Marketing Category Name | NDA |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | DOBUTAMINE HYDROCHLORIDE |
Strength Number | 400 |
Strength Unit | mg/100mL |
Pharmaceutical Classes | Adrenergic beta-Agonists [MoA],beta-Adrenergic Agonist [EPC] |