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Dobutamine Hydrochloride in Dextrose - 0338-1073-03 - (Dobutamine Hydrochloride)

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Drug Information of Dobutamine Hydrochloride in Dextrose

Product NDC: 0338-1073
Proprietary Name: Dobutamine Hydrochloride in Dextrose
Non Proprietary Name: Dobutamine Hydrochloride
Active Ingredient(s): 100    mg/100mL & nbsp;   Dobutamine Hydrochloride
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Dobutamine Hydrochloride in Dextrose

Product NDC: 0338-1073
Labeler Name: Baxter Healthcare Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020255
Marketing Category: NDA
Start Marketing Date: 19930927

Package Information of Dobutamine Hydrochloride in Dextrose

Package NDC: 0338-1073-03
Package Description: 500 mL in 1 BAG (0338-1073-03)

NDC Information of Dobutamine Hydrochloride in Dextrose

NDC Code 0338-1073-03
Proprietary Name Dobutamine Hydrochloride in Dextrose
Package Description 500 mL in 1 BAG (0338-1073-03)
Product NDC 0338-1073
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Dobutamine Hydrochloride
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 19930927
Marketing Category Name NDA
Labeler Name Baxter Healthcare Corporation
Substance Name DOBUTAMINE HYDROCHLORIDE
Strength Number 100
Strength Unit mg/100mL
Pharmaceutical Classes Adrenergic beta-Agonists [MoA],beta-Adrenergic Agonist [EPC]

Complete Information of Dobutamine Hydrochloride in Dextrose


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