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DOBUTamine Hydrochloride in Dextrose - 0409-2347-32 - (DOBUTAMINE HYDROCHLORIDE)

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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]

Complete Information of DOBUTamine Hydrochloride in Dextrose


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