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Vancomycin Hydrochloride - 0409-6509-01 - (VANCOMYCIN HYDROCHLORIDE)

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Drug Information of Vancomycin Hydrochloride

Product NDC: 0409-6509
Proprietary Name: Vancomycin Hydrochloride
Non Proprietary Name: VANCOMYCIN HYDROCHLORIDE
Active Ingredient(s): 500    mg/10mL & nbsp;   VANCOMYCIN HYDROCHLORIDE
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Vancomycin Hydrochloride

Product NDC: 0409-6509
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA063076
Marketing Category: ANDA
Start Marketing Date: 20100604

Package Information of Vancomycin Hydrochloride

Package NDC: 0409-6509-01
Package Description: 1 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (0409-6509-01) > 100 mL in 1 VIAL, PHARMACY BULK PACKAGE

NDC Information of Vancomycin Hydrochloride

NDC Code 0409-6509-01
Proprietary Name Vancomycin Hydrochloride
Package Description 1 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (0409-6509-01) > 100 mL in 1 VIAL, PHARMACY BULK PACKAGE
Product NDC 0409-6509
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name VANCOMYCIN HYDROCHLORIDE
Dosage Form Name INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20100604
Marketing Category Name ANDA
Labeler Name Hospira, Inc.
Substance Name VANCOMYCIN HYDROCHLORIDE
Strength Number 500
Strength Unit mg/10mL
Pharmaceutical Classes Glycopeptide Antibacterial [EPC],Glycopeptides [Chemical/Ingredient]

Complete Information of Vancomycin Hydrochloride


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