Home > National Drug Code (NDC) > Ceftriaxone Sodium

Ceftriaxone Sodium - 54868-5533-0 - (Ceftriaxone Sodium)

Alphabetical Index


Drug Information of Ceftriaxone Sodium

Product NDC: 54868-5533
Proprietary Name: Ceftriaxone Sodium
Non Proprietary Name: Ceftriaxone Sodium
Active Ingredient(s): 500    mg/1 & nbsp;   Ceftriaxone Sodium
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Ceftriaxone Sodium

Product NDC: 54868-5533
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065230
Marketing Category: ANDA
Start Marketing Date: 20080115

Package Information of Ceftriaxone Sodium

Package NDC: 54868-5533-0
Package Description: 10 VIAL in 1 BOX (54868-5533-0) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL

NDC Information of Ceftriaxone Sodium

NDC Code 54868-5533-0
Proprietary Name Ceftriaxone Sodium
Package Description 10 VIAL in 1 BOX (54868-5533-0) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
Product NDC 54868-5533
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ceftriaxone Sodium
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20080115
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name CEFTRIAXONE SODIUM
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of Ceftriaxone Sodium


General Information