Cefepime - 0338-1301-41 - (cefepime)

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Drug Information of Cefepime

Product NDC: 0338-1301
Proprietary Name: Cefepime
Non Proprietary Name: cefepime
Active Ingredient(s): 1    g/50mL & nbsp;   cefepime
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Cefepime

Product NDC: 0338-1301
Labeler Name: Baxter Healthcare Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050817
Marketing Category: NDA
Start Marketing Date: 20080805

Package Information of Cefepime

Package NDC: 0338-1301-41
Package Description: 24 BAG in 1 BOX (0338-1301-41) > 50 mL in 1 BAG

NDC Information of Cefepime

NDC Code 0338-1301-41
Proprietary Name Cefepime
Package Description 24 BAG in 1 BOX (0338-1301-41) > 50 mL in 1 BAG
Product NDC 0338-1301
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name cefepime
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20080805
Marketing Category Name NDA
Labeler Name Baxter Healthcare Corporation
Substance Name CEFEPIME HYDROCHLORIDE
Strength Number 1
Strength Unit g/50mL
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of Cefepime


General Information