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Ceftriaxone Sodium - 0409-7334-10 - (Ceftriaxone Sodium)

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Drug Information of Ceftriaxone Sodium

Product NDC: 0409-7334
Proprietary Name: Ceftriaxone Sodium
Non Proprietary Name: Ceftriaxone Sodium
Active Ingredient(s): 10    g/100mL & nbsp;   Ceftriaxone Sodium
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Ceftriaxone Sodium

Product NDC: 0409-7334
Labeler Name: Hospira, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065168
Marketing Category: ANDA
Start Marketing Date: 20050517

Package Information of Ceftriaxone Sodium

Package NDC: 0409-7334-10
Package Description: 1 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (0409-7334-10) > 100 mL in 1 VIAL, PHARMACY BULK PACKAGE

NDC Information of Ceftriaxone Sodium

NDC Code 0409-7334-10
Proprietary Name Ceftriaxone Sodium
Package Description 1 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (0409-7334-10) > 100 mL in 1 VIAL, PHARMACY BULK PACKAGE
Product NDC 0409-7334
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ceftriaxone Sodium
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20050517
Marketing Category Name ANDA
Labeler Name Hospira, Inc
Substance Name CEFTRIAXONE SODIUM
Strength Number 10
Strength Unit g/100mL
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of Ceftriaxone Sodium


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