Cefepime - 63323-340-20 - (Cefepime)

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Drug Information of Cefepime

Product NDC: 63323-340
Proprietary Name: Cefepime
Non Proprietary Name: Cefepime
Active Ingredient(s): 2    g/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: 63323-340
Labeler Name: APP Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065441
Marketing Category: ANDA
Start Marketing Date: 20100830

Package Information of Cefepime

Package NDC: 63323-340-20
Package Description: 10 VIAL in 1 CARTON (63323-340-20) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL

NDC Information of Cefepime

NDC Code 63323-340-20
Proprietary Name Cefepime
Package Description 10 VIAL in 1 CARTON (63323-340-20) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
Product NDC 63323-340
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cefepime
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20100830
Marketing Category Name ANDA
Labeler Name APP Pharmaceuticals, LLC
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