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Ceftriaxone Sodium - 55154-6957-5 - (Ceftriaxone Sodium)

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Drug Information of Ceftriaxone Sodium

Product NDC: 55154-6957
Proprietary Name: Ceftriaxone Sodium
Non Proprietary Name: Ceftriaxone Sodium
Active Ingredient(s): 2    g/1 & 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: 55154-6957
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065204
Marketing Category: ANDA
Start Marketing Date: 20050503

Package Information of Ceftriaxone Sodium

Package NDC: 55154-6957-5
Package Description: 5 VIAL, SINGLE-USE in 1 BAG (55154-6957-5) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE

NDC Information of Ceftriaxone Sodium

NDC Code 55154-6957-5
Proprietary Name Ceftriaxone Sodium
Package Description 5 VIAL, SINGLE-USE in 1 BAG (55154-6957-5) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE
Product NDC 55154-6957
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ceftriaxone Sodium
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20050503
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name CEFTRIAXONE SODIUM
Strength Number 2
Strength Unit g/1
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of Ceftriaxone Sodium


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