Cefazolin - 60505-0749-4 - (Cefazolin)

Alphabetical Index


Drug Information of Cefazolin

Product NDC: 60505-0749
Proprietary Name: Cefazolin
Non Proprietary Name: Cefazolin
Active Ingredient(s): 1    g/1 & nbsp;   Cefazolin
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Cefazolin

Product NDC: 60505-0749
Labeler Name: Apotex Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065226
Marketing Category: ANDA
Start Marketing Date: 20051007

Package Information of Cefazolin

Package NDC: 60505-0749-4
Package Description: 10 VIAL in 1 CARTON (60505-0749-4) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL

NDC Information of Cefazolin

NDC Code 60505-0749-4
Proprietary Name Cefazolin
Package Description 10 VIAL in 1 CARTON (60505-0749-4) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
Product NDC 60505-0749
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cefazolin
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20051007
Marketing Category Name ANDA
Labeler Name Apotex Corp
Substance Name CEFAZOLIN SODIUM
Strength Number 1
Strength Unit g/1
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of Cefazolin


General Information