cefepime - 60505-6031-4 - (cefepime)

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Drug Information of cefepime

Product NDC: 60505-6031
Proprietary Name: cefepime
Non Proprietary Name: cefepime
Active Ingredient(s): 2    g/1 & nbsp;   cefepime
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of cefepime

Product NDC: 60505-6031
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065369
Marketing Category: ANDA
Start Marketing Date: 20080314

Package Information of cefepime

Package NDC: 60505-6031-4
Package Description: 10 VIAL in 1 BOX (60505-6031-4) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL

NDC Information of cefepime

NDC Code 60505-6031-4
Proprietary Name cefepime
Package Description 10 VIAL in 1 BOX (60505-6031-4) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
Product NDC 60505-6031
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name cefepime
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20080314
Marketing Category Name ANDA
Labeler Name Apotex Corp.
Substance Name CEFEPIME HYDROCHLORIDE
Strength Number 2
Strength Unit g/1
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of cefepime


General Information