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Cefepime Hydrochloride - 0781-3222-95 - (Cefepime Hydrochloride)

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Drug Information of Cefepime Hydrochloride

Product NDC: 0781-3222
Proprietary Name: Cefepime Hydrochloride
Non Proprietary Name: Cefepime Hydrochloride
Active Ingredient(s): 1    g/1 & nbsp;   Cefepime Hydrochloride
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Cefepime Hydrochloride

Product NDC: 0781-3222
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065441
Marketing Category: ANDA
Start Marketing Date: 20080501

Package Information of Cefepime Hydrochloride

Package NDC: 0781-3222-95
Package Description: 10 VIAL, SINGLE-DOSE in 1 CARTON (0781-3222-95) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (0781-3222-80)

NDC Information of Cefepime Hydrochloride

NDC Code 0781-3222-95
Proprietary Name Cefepime Hydrochloride
Package Description 10 VIAL, SINGLE-DOSE in 1 CARTON (0781-3222-95) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (0781-3222-80)
Product NDC 0781-3222
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cefepime Hydrochloride
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20080501
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name CEFEPIME HYDROCHLORIDE
Strength Number 1
Strength Unit g/1
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of Cefepime Hydrochloride


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