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Ceftriaxone - 68330-002-10 - (Ceftriaxone)

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Drug Information of Ceftriaxone

Product NDC: 68330-002
Proprietary Name: Ceftriaxone
Non Proprietary Name: Ceftriaxone
Active Ingredient(s): 500    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: 68330-002
Labeler Name: Cephazone Pharma LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065294
Marketing Category: ANDA
Start Marketing Date: 20080715

Package Information of Ceftriaxone

Package NDC: 68330-002-10
Package Description: 10 BOX in 1 CARTON (68330-002-10) > 1 VIAL, GLASS in 1 BOX (68330-002-01) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, GLASS

NDC Information of Ceftriaxone

NDC Code 68330-002-10
Proprietary Name Ceftriaxone
Package Description 10 BOX in 1 CARTON (68330-002-10) > 1 VIAL, GLASS in 1 BOX (68330-002-01) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, GLASS
Product NDC 68330-002
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ceftriaxone
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20080715
Marketing Category Name ANDA
Labeler Name Cephazone Pharma LLC
Substance Name CEFTRIAXONE SODIUM
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

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