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Ceftriaxone - 25021-106-10 - (ceftriaxone)

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Drug Information of Ceftriaxone

Product NDC: 25021-106
Proprietary Name: Ceftriaxone
Non Proprietary Name: ceftriaxone
Active Ingredient(s): 1    g/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: 25021-106
Labeler Name: Sagent Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065329
Marketing Category: ANDA
Start Marketing Date: 20091105

Package Information of Ceftriaxone

Package NDC: 25021-106-10
Package Description: 25 VIAL in 1 CARTON (25021-106-10) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL

NDC Information of Ceftriaxone

NDC Code 25021-106-10
Proprietary Name Ceftriaxone
Package Description 25 VIAL in 1 CARTON (25021-106-10) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
Product NDC 25021-106
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ceftriaxone
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20091105
Marketing Category Name ANDA
Labeler Name Sagent Pharmaceuticals
Substance Name CEFTRIAXONE SODIUM
Strength Number 1
Strength Unit g/1
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of Ceftriaxone


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