cefepime - 60505-0678-0 - (cefepime)

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Drug Information of cefepime

Product NDC: 60505-0678
Proprietary Name: cefepime
Non Proprietary Name: cefepime
Active Ingredient(s): 500    mg/1 & nbsp;   cefepime
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of cefepime

Product NDC: 60505-0678
Labeler Name: APOTEX CORP.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065369
Marketing Category: ANDA
Start Marketing Date: 20070305

Package Information of cefepime

Package NDC: 60505-0678-0
Package Description: 1 VIAL in 1 BOX (60505-0678-0) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL

NDC Information of cefepime

NDC Code 60505-0678-0
Proprietary Name cefepime
Package Description 1 VIAL in 1 BOX (60505-0678-0) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
Product NDC 60505-0678
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name cefepime
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20070305
Marketing Category Name ANDA
Labeler Name APOTEX CORP.
Substance Name CEFEPIME HYDROCHLORIDE
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of cefepime


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