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VANCOMYCIN HYDROCHLORIDE - 0338-3551-48 - (VANCOMYCIN HYDROCHLORIDE)

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Drug Information of VANCOMYCIN HYDROCHLORIDE

Product NDC: 0338-3551
Proprietary Name: VANCOMYCIN HYDROCHLORIDE
Non Proprietary Name: VANCOMYCIN HYDROCHLORIDE
Active Ingredient(s): 500    mg/100mL & nbsp;   VANCOMYCIN HYDROCHLORIDE
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of VANCOMYCIN HYDROCHLORIDE

Product NDC: 0338-3551
Labeler Name: Baxter Healthcare Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050671
Marketing Category: NDA
Start Marketing Date: 20120117

Package Information of VANCOMYCIN HYDROCHLORIDE

Package NDC: 0338-3551-48
Package Description: 100 mL in 1 BAG (0338-3551-48)

NDC Information of VANCOMYCIN HYDROCHLORIDE

NDC Code 0338-3551-48
Proprietary Name VANCOMYCIN HYDROCHLORIDE
Package Description 100 mL in 1 BAG (0338-3551-48)
Product NDC 0338-3551
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name VANCOMYCIN HYDROCHLORIDE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20120117
Marketing Category Name NDA
Labeler Name Baxter Healthcare Corporation
Substance Name VANCOMYCIN HYDROCHLORIDE
Strength Number 500
Strength Unit mg/100mL
Pharmaceutical Classes Glycopeptide Antibacterial [EPC],Glycopeptides [Chemical/Ingredient]

Complete Information of VANCOMYCIN HYDROCHLORIDE


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