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Ceftriaxone Sodium - 60505-6088-1 - (Ceftriaxone Sodium)

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Drug Information of Ceftriaxone Sodium

Product NDC: 60505-6088
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: 60505-6088
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065231
Marketing Category: ANDA
Start Marketing Date: 20050802

Package Information of Ceftriaxone Sodium

Package NDC: 60505-6088-1
Package Description: 1 BOTTLE in 1 BOX (60505-6088-1) > 1 INJECTION, POWDER, FOR SOLUTION in 1 BOTTLE

NDC Information of Ceftriaxone Sodium

NDC Code 60505-6088-1
Proprietary Name Ceftriaxone Sodium
Package Description 1 BOTTLE in 1 BOX (60505-6088-1) > 1 INJECTION, POWDER, FOR SOLUTION in 1 BOTTLE
Product NDC 60505-6088
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ceftriaxone Sodium
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20050802
Marketing Category Name ANDA
Labeler Name Apotex Corp.
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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