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Ceftriaxone - 55154-0375-8 - (Ceftriaxone)

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Drug Information of Ceftriaxone

Product NDC: 55154-0375
Proprietary Name: Ceftriaxone
Non Proprietary Name: Ceftriaxone
Active Ingredient(s): 500    mg/1 & nbsp;   Ceftriaxone
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Ceftriaxone

Product NDC: 55154-0375
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065465
Marketing Category: ANDA
Start Marketing Date: 20090722

Package Information of Ceftriaxone

Package NDC: 55154-0375-8
Package Description: 1 VIAL in 1 BAG (55154-0375-8) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL

NDC Information of Ceftriaxone

NDC Code 55154-0375-8
Proprietary Name Ceftriaxone
Package Description 1 VIAL in 1 BAG (55154-0375-8) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
Product NDC 55154-0375
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ceftriaxone
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20090722
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name CEFTRIAXONE SODIUM
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of Ceftriaxone


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