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Ceftriaxone - 25021-108-99 - (CEFTRIAXONE Sodium)

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Drug Information of Ceftriaxone

Product NDC: 25021-108
Proprietary Name: Ceftriaxone
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

Product NDC: 25021-108
Labeler Name: Sagent Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065328
Marketing Category: ANDA
Start Marketing Date: 20091105

Package Information of Ceftriaxone

Package NDC: 25021-108-99
Package Description: 1 BOTTLE in 1 CARTON (25021-108-99) > 100 mL in 1 BOTTLE

NDC Information of Ceftriaxone

NDC Code 25021-108-99
Proprietary Name Ceftriaxone
Package Description 1 BOTTLE in 1 CARTON (25021-108-99) > 100 mL in 1 BOTTLE
Product NDC 25021-108
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CEFTRIAXONE Sodium
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20091105
Marketing Category Name ANDA
Labeler Name Sagent Pharmaceuticals
Substance Name CEFTRIAXONE SODIUM
Strength Number 10
Strength Unit g/100mL
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of Ceftriaxone


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