Cefepime - 0409-0809-01 - (CEFEPIME HYDROCHLORIDE)

Alphabetical Index


Drug Information of Cefepime

Product NDC: 0409-0809
Proprietary Name: Cefepime
Non Proprietary Name: CEFEPIME HYDROCHLORIDE
Active Ingredient(s): 1    g/1 & nbsp;   CEFEPIME HYDROCHLORIDE
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Cefepime

Product NDC: 0409-0809
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA202268
Marketing Category: ANDA
Start Marketing Date: 20120730

Package Information of Cefepime

Package NDC: 0409-0809-01
Package Description: 25 VIAL in 1 CARTON (0409-0809-01) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL

NDC Information of Cefepime

NDC Code 0409-0809-01
Proprietary Name Cefepime
Package Description 25 VIAL in 1 CARTON (0409-0809-01) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
Product NDC 0409-0809
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CEFEPIME HYDROCHLORIDE
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20120730
Marketing Category Name ANDA
Labeler Name Hospira, Inc.
Substance Name CEFEPIME HYDROCHLORIDE
Strength Number 1
Strength Unit g/1
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of Cefepime


General Information