Cefazolin - 0409-0806-01 - (Cefazolin)

Alphabetical Index


Drug Information of Cefazolin

Product NDC: 0409-0806
Proprietary Name: Cefazolin
Non Proprietary Name: Cefazolin
Active Ingredient(s): 10    g/1 & nbsp;   Cefazolin
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Cefazolin

Product NDC: 0409-0806
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065247
Marketing Category: ANDA
Start Marketing Date: 20090324

Package Information of Cefazolin

Package NDC: 0409-0806-01
Package Description: 10 BOTTLE in 1 CARTON (0409-0806-01) > 1 INJECTION, POWDER, FOR SOLUTION in 1 BOTTLE

NDC Information of Cefazolin

NDC Code 0409-0806-01
Proprietary Name Cefazolin
Package Description 10 BOTTLE in 1 CARTON (0409-0806-01) > 1 INJECTION, POWDER, FOR SOLUTION in 1 BOTTLE
Product NDC 0409-0806
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cefazolin
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20090324
Marketing Category Name ANDA
Labeler Name Hospira, Inc.
Substance Name CEFAZOLIN SODIUM
Strength Number 10
Strength Unit g/1
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of Cefazolin


General Information