Cefazolin - 68258-8978-2 - (cefazolin sodium)

Alphabetical Index


Drug Information of Cefazolin

Product NDC: 68258-8978
Proprietary Name: Cefazolin
Non Proprietary Name: cefazolin sodium
Active Ingredient(s): 1    g/3mL & nbsp;   cefazolin sodium
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Cefazolin

Product NDC: 68258-8978
Labeler Name: Dispensing Solutions, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA063207
Marketing Category: ANDA
Start Marketing Date: 20090201

Package Information of Cefazolin

Package NDC: 68258-8978-2
Package Description: 25 VIAL in 1 CARTON (68258-8978-2) > 3 mL in 1 VIAL

NDC Information of Cefazolin

NDC Code 68258-8978-2
Proprietary Name Cefazolin
Package Description 25 VIAL in 1 CARTON (68258-8978-2) > 3 mL in 1 VIAL
Product NDC 68258-8978
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name cefazolin sodium
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20090201
Marketing Category Name ANDA
Labeler Name Dispensing Solutions, Inc.
Substance Name CEFAZOLIN SODIUM
Strength Number 1
Strength Unit g/3mL
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of Cefazolin


General Information