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Ceftriaxone Sodium - 0409-7338-01 - (Ceftriaxone Sodium)

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Drug Information of Ceftriaxone Sodium

Product NDC: 0409-7338
Proprietary Name: Ceftriaxone Sodium
Non Proprietary Name: Ceftriaxone Sodium
Active Ingredient(s): 500    mg/1 & nbsp;   Ceftriaxone Sodium
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Ceftriaxone Sodium

Product NDC: 0409-7338
Labeler Name: Hospira, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065169
Marketing Category: ANDA
Start Marketing Date: 20050509

Package Information of Ceftriaxone Sodium

Package NDC: 0409-7338-01
Package Description: 10 VIAL, SINGLE-USE in 1 CARTON (0409-7338-01) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE

NDC Information of Ceftriaxone Sodium

NDC Code 0409-7338-01
Proprietary Name Ceftriaxone Sodium
Package Description 10 VIAL, SINGLE-USE in 1 CARTON (0409-7338-01) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE
Product NDC 0409-7338
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ceftriaxone Sodium
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20050509
Marketing Category Name ANDA
Labeler Name Hospira, Inc
Substance Name CEFTRIAXONE SODIUM
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of Ceftriaxone Sodium


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