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Vancomycin Hydrochloride - 63323-295-61 - (VANCOMYCIN HYDROCHLORIDE)

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Drug Information of Vancomycin Hydrochloride

Product NDC: 63323-295
Proprietary Name: Vancomycin Hydrochloride
Non Proprietary Name: VANCOMYCIN HYDROCHLORIDE
Active Ingredient(s): 5    g/100mL & 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: 63323-295
Labeler Name: APP Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA062663
Marketing Category: ANDA
Start Marketing Date: 20010717

Package Information of Vancomycin Hydrochloride

Package NDC: 63323-295-61
Package Description: 1 BOTTLE in 1 CARTON (63323-295-61) > 100 mL in 1 BOTTLE

NDC Information of Vancomycin Hydrochloride

NDC Code 63323-295-61
Proprietary Name Vancomycin Hydrochloride
Package Description 1 BOTTLE in 1 CARTON (63323-295-61) > 100 mL in 1 BOTTLE
Product NDC 63323-295
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 20010717
Marketing Category Name ANDA
Labeler Name APP Pharmaceuticals, LLC
Substance Name VANCOMYCIN HYDROCHLORIDE
Strength Number 5
Strength Unit g/100mL
Pharmaceutical Classes Glycopeptide Antibacterial [EPC],Glycopeptides [Chemical/Ingredient]

Complete Information of Vancomycin Hydrochloride


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