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DOBUTamine Hydrochloride in Dextrose
DOBUTamine Hydrochloride in Dextrose - 0409-2347-32 - (DOBUTAMINE HYDROCHLORIDE)
Drug Information of DOBUTamine Hydrochloride in Dextrose
| Product NDC: | 0409-2347 |
| Proprietary Name: | DOBUTamine Hydrochloride in Dextrose |
| Non Proprietary Name: | DOBUTAMINE HYDROCHLORIDE |
| Active Ingredient(s): | 200 mg/100mL & nbsp; DOBUTAMINE HYDROCHLORIDE |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DOBUTamine Hydrochloride in Dextrose
| Product NDC: | 0409-2347 |
| Labeler Name: | Hospira, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020201 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20111011 |
Package Information of DOBUTamine Hydrochloride in Dextrose
| Package NDC: | 0409-2347-32 |
| Package Description: | 12 POUCH in 1 CASE (0409-2347-32) > 1 BAG in 1 POUCH > 250 mL in 1 BAG |
NDC Information of DOBUTamine Hydrochloride in Dextrose
| NDC Code | 0409-2347-32 |
| Proprietary Name | DOBUTamine Hydrochloride in Dextrose |
| Package Description | 12 POUCH in 1 CASE (0409-2347-32) > 1 BAG in 1 POUCH > 250 mL in 1 BAG |
| Product NDC | 0409-2347 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | DOBUTAMINE HYDROCHLORIDE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20111011 |
| Marketing Category Name | NDA |
| Labeler Name | Hospira, Inc. |
| Substance Name | DOBUTAMINE HYDROCHLORIDE |
| Strength Number | 200 |
| Strength Unit | mg/100mL |
| Pharmaceutical Classes | Adrenergic beta-Agonists [MoA],beta-Adrenergic Agonist [EPC] |
