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DOBUTAMINE HYDROCHLORIDE - 0409-2344-02 - (DOBUTAMINE HYDROCHLORIDE)

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Drug Information of DOBUTAMINE HYDROCHLORIDE

Product NDC: 0409-2344
Proprietary Name: DOBUTAMINE HYDROCHLORIDE
Non Proprietary Name: DOBUTAMINE HYDROCHLORIDE
Active Ingredient(s): 12.5    mg/mL & nbsp;   DOBUTAMINE HYDROCHLORIDE
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION, CONCENTRATE
Coding System: National Drug Codes(NDC)

Labeler Information of DOBUTAMINE HYDROCHLORIDE

Product NDC: 0409-2344
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074086
Marketing Category: ANDA
Start Marketing Date: 20110625

Package Information of DOBUTAMINE HYDROCHLORIDE

Package NDC: 0409-2344-02
Package Description: 10 VIAL, SINGLE-DOSE in 1 TRAY (0409-2344-02) > 20 mL in 1 VIAL, SINGLE-DOSE

NDC Information of DOBUTAMINE HYDROCHLORIDE

NDC Code 0409-2344-02
Proprietary Name DOBUTAMINE HYDROCHLORIDE
Package Description 10 VIAL, SINGLE-DOSE in 1 TRAY (0409-2344-02) > 20 mL in 1 VIAL, SINGLE-DOSE
Product NDC 0409-2344
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name DOBUTAMINE HYDROCHLORIDE
Dosage Form Name INJECTION, SOLUTION, CONCENTRATE
Route Name INTRAVENOUS
Start Marketing Date 20110625
Marketing Category Name ANDA
Labeler Name Hospira, Inc.
Substance Name DOBUTAMINE HYDROCHLORIDE
Strength Number 12.5
Strength Unit mg/mL
Pharmaceutical Classes Adrenergic beta-Agonists [MoA],beta-Adrenergic Agonist [EPC]

Complete Information of DOBUTAMINE HYDROCHLORIDE


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