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Vancomycin Hydrochloride - 0409-6535-01 - (VANCOMYCIN HYDROCHLORIDE)

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Drug Information of Vancomycin Hydrochloride

Product NDC: 0409-6535
Proprietary Name: Vancomycin Hydrochloride
Non Proprietary Name: VANCOMYCIN HYDROCHLORIDE
Active Ingredient(s): 1    g/250mL & 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: 0409-6535
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA062933
Marketing Category: ANDA
Start Marketing Date: 20100729

Package Information of Vancomycin Hydrochloride

Package NDC: 0409-6535-01
Package Description: 10 VIAL, SINGLE-DOSE in 1 TRAY (0409-6535-01) > 250 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Vancomycin Hydrochloride

NDC Code 0409-6535-01
Proprietary Name Vancomycin Hydrochloride
Package Description 10 VIAL, SINGLE-DOSE in 1 TRAY (0409-6535-01) > 250 mL in 1 VIAL, SINGLE-DOSE
Product NDC 0409-6535
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 20100729
Marketing Category Name ANDA
Labeler Name Hospira, Inc.
Substance Name VANCOMYCIN HYDROCHLORIDE
Strength Number 1
Strength Unit g/250mL
Pharmaceutical Classes Glycopeptide Antibacterial [EPC],Glycopeptides [Chemical/Ingredient]

Complete Information of Vancomycin Hydrochloride


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