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Vancomycin Hydrochloride - 63323-338-20 - (VANCOMYCIN HYDROCHLORIDE)

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Drug Information of Vancomycin Hydrochloride

Product NDC: 63323-338
Proprietary Name: Vancomycin Hydrochloride
Non Proprietary Name: VANCOMYCIN HYDROCHLORIDE
Active Ingredient(s): 125    mg/1 & nbsp;   VANCOMYCIN HYDROCHLORIDE
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Vancomycin Hydrochloride

Product NDC: 63323-338
Labeler Name: APP Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065453
Marketing Category: ANDA
Start Marketing Date: 20120618

Package Information of Vancomycin Hydrochloride

Package NDC: 63323-338-20
Package Description: 2 BLISTER PACK in 1 CARTON (63323-338-20) > 10 CAPSULE in 1 BLISTER PACK

NDC Information of Vancomycin Hydrochloride

NDC Code 63323-338-20
Proprietary Name Vancomycin Hydrochloride
Package Description 2 BLISTER PACK in 1 CARTON (63323-338-20) > 10 CAPSULE in 1 BLISTER PACK
Product NDC 63323-338
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name VANCOMYCIN HYDROCHLORIDE
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20120618
Marketing Category Name ANDA
Labeler Name APP Pharmaceuticals, LLC
Substance Name VANCOMYCIN HYDROCHLORIDE
Strength Number 125
Strength Unit mg/1
Pharmaceutical Classes Glycopeptide Antibacterial [EPC],Glycopeptides [Chemical/Ingredient]

Complete Information of Vancomycin Hydrochloride


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