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VANCOMYCIN HYDROCHLORIDE - 63323-221-10 - (VANCOMYCIN HYDROCHLORIDE)

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Drug Information of VANCOMYCIN HYDROCHLORIDE

Product NDC: 63323-221
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: 63323-221
Labeler Name: APP Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA062663
Marketing Category: ANDA
Start Marketing Date: 20000901

Package Information of VANCOMYCIN HYDROCHLORIDE

Package NDC: 63323-221-10
Package Description: 25 VIAL in 1 TRAY (63323-221-10) > 10 mL in 1 VIAL

NDC Information of VANCOMYCIN HYDROCHLORIDE

NDC Code 63323-221-10
Proprietary Name VANCOMYCIN HYDROCHLORIDE
Package Description 25 VIAL in 1 TRAY (63323-221-10) > 10 mL in 1 VIAL
Product NDC 63323-221
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 20000901
Marketing Category Name ANDA
Labeler Name APP Pharmaceuticals, LLC
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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