Home > National Drug Code (NDC) > CEFTRIAXONE

CEFTRIAXONE - 64679-701-03 - (CEFTRIAXONE)

Alphabetical Index


Drug Information of CEFTRIAXONE

Product NDC: 64679-701
Proprietary Name: CEFTRIAXONE
Non Proprietary Name: CEFTRIAXONE
Active Ingredient(s): 250    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: 64679-701
Labeler Name: Wockhardt USA LLC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065391
Marketing Category: ANDA
Start Marketing Date: 20070412

Package Information of CEFTRIAXONE

Package NDC: 64679-701-03
Package Description: 25 INJECTION, POWDER, FOR SOLUTION in 1 BOX (64679-701-03)

NDC Information of CEFTRIAXONE

NDC Code 64679-701-03
Proprietary Name CEFTRIAXONE
Package Description 25 INJECTION, POWDER, FOR SOLUTION in 1 BOX (64679-701-03)
Product NDC 64679-701
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CEFTRIAXONE
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20070412
Marketing Category Name ANDA
Labeler Name Wockhardt USA LLC.
Substance Name CEFTRIAXONE SODIUM
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of CEFTRIAXONE


General Information