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Dopamine Hydrochloride and Dextrose - 0338-1009-02 - (Dopamine Hydrochloride)

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Drug Information of Dopamine Hydrochloride and Dextrose

Product NDC: 0338-1009
Proprietary Name: Dopamine Hydrochloride and Dextrose
Non Proprietary Name: Dopamine Hydrochloride
Active Ingredient(s): 320    mg/100mL & nbsp;   Dopamine Hydrochloride
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Dopamine Hydrochloride and Dextrose

Product NDC: 0338-1009
Labeler Name: Baxter Healthcare Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019615
Marketing Category: NDA
Start Marketing Date: 20120125

Package Information of Dopamine Hydrochloride and Dextrose

Package NDC: 0338-1009-02
Package Description: 250 mL in 1 BAG (0338-1009-02)

NDC Information of Dopamine Hydrochloride and Dextrose

NDC Code 0338-1009-02
Proprietary Name Dopamine Hydrochloride and Dextrose
Package Description 250 mL in 1 BAG (0338-1009-02)
Product NDC 0338-1009
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Dopamine Hydrochloride
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20120125
Marketing Category Name NDA
Labeler Name Baxter Healthcare Corporation
Substance Name DOPAMINE HYDROCHLORIDE
Strength Number 320
Strength Unit mg/100mL
Pharmaceutical Classes Catecholamine [EPC],Catecholamines [Chemical/Ingredient]

Complete Information of Dopamine Hydrochloride and Dextrose


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