Vancocin - 66593-3125-2 - (vancomycin hydrochloride)

Alphabetical Index


Drug Information of Vancocin

Product NDC: 66593-3125
Proprietary Name: Vancocin
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 Vancocin

Product NDC: 66593-3125
Labeler Name: ViroPharma
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050606
Marketing Category: NDA
Start Marketing Date: 19860415

Package Information of Vancocin

Package NDC: 66593-3125-2
Package Description: 2 BLISTER PACK in 1 BOX (66593-3125-2) > 10 CAPSULE in 1 BLISTER PACK

NDC Information of Vancocin

NDC Code 66593-3125-2
Proprietary Name Vancocin
Package Description 2 BLISTER PACK in 1 BOX (66593-3125-2) > 10 CAPSULE in 1 BLISTER PACK
Product NDC 66593-3125
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name vancomycin hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19860415
Marketing Category Name NDA
Labeler Name ViroPharma
Substance Name VANCOMYCIN HYDROCHLORIDE
Strength Number 125
Strength Unit mg/1
Pharmaceutical Classes Glycopeptide Antibacterial [EPC],Glycopeptides [Chemical/Ingredient]

Complete Information of Vancocin


General Information