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Vancomycin Hydrochloride - 0069-2587-10 - (VANCOMYCIN HYDROCHLORIDE)

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Drug Information of Vancomycin Hydrochloride

Product NDC: 0069-2587
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: 0069-2587
Labeler Name: Pfizer Laboratories Div Pfizer Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065397
Marketing Category: ANDA
Start Marketing Date: 20110510

Package Information of Vancomycin Hydrochloride

Package NDC: 0069-2587-10
Package Description: 10 VIAL in 1 CARTON (0069-2587-10) > 10 mL in 1 VIAL (0069-2587-03)

NDC Information of Vancomycin Hydrochloride

NDC Code 0069-2587-10
Proprietary Name Vancomycin Hydrochloride
Package Description 10 VIAL in 1 CARTON (0069-2587-10) > 10 mL in 1 VIAL (0069-2587-03)
Product NDC 0069-2587
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 20110510
Marketing Category Name ANDA
Labeler Name Pfizer Laboratories Div Pfizer 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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