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Vancomycin Hydrochloride - 17478-742-02 - (Vancomycin Hydrochloride)

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Drug Information of Vancomycin Hydrochloride

Product NDC: 17478-742
Proprietary Name: Vancomycin Hydrochloride
Non Proprietary Name: Vancomycin Hydrochloride
Active Ingredient(s): 250    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: 17478-742
Labeler Name: Akorn, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065478
Marketing Category: ANDA
Start Marketing Date: 20120409

Package Information of Vancomycin Hydrochloride

Package NDC: 17478-742-02
Package Description: 2 BLISTER PACK in 1 CARTON (17478-742-02) > 10 CAPSULE in 1 BLISTER PACK

NDC Information of Vancomycin Hydrochloride

NDC Code 17478-742-02
Proprietary Name Vancomycin Hydrochloride
Package Description 2 BLISTER PACK in 1 CARTON (17478-742-02) > 10 CAPSULE in 1 BLISTER PACK
Product NDC 17478-742
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Vancomycin Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20120409
Marketing Category Name ANDA
Labeler Name Akorn, Inc.
Substance Name VANCOMYCIN HYDROCHLORIDE
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes Glycopeptide Antibacterial [EPC],Glycopeptides [Chemical/Ingredient]

Complete Information of Vancomycin Hydrochloride


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