Home
>
National Drug Code (NDC)
>
Dobutamine
Dobutamine - 54868-5717-1 - (Dobutamine Hydrochloride)
Drug Information of Dobutamine
| Product NDC: | 54868-5717 |
| Proprietary Name: | Dobutamine |
| Non Proprietary Name: | Dobutamine Hydrochloride |
| Active Ingredient(s): | 12.5 mg/mL & nbsp; Dobutamine Hydrochloride |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dobutamine
| Product NDC: | 54868-5717 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074292 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20061211 |
Package Information of Dobutamine
| Package NDC: | 54868-5717-1 |
| Package Description: | 10 VIAL, SINGLE-DOSE in 1 BOX (54868-5717-1) > 40 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of Dobutamine
| NDC Code | 54868-5717-1 |
| Proprietary Name | Dobutamine |
| Package Description | 10 VIAL, SINGLE-DOSE in 1 BOX (54868-5717-1) > 40 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 54868-5717 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Dobutamine Hydrochloride |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20061211 |
| Marketing Category Name | ANDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | DOBUTAMINE HYDROCHLORIDE |
| Strength Number | 12.5 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Adrenergic beta-Agonists [MoA],beta-Adrenergic Agonist [EPC] |
