Cefazolin - 0409-0805-01 - (Cefazolin)

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Drug Information of Cefazolin

Product NDC: 0409-0805
Proprietary Name: Cefazolin
Non Proprietary Name: Cefazolin
Active Ingredient(s): 1    g/3mL & 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: 0409-0805
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065226
Marketing Category: ANDA
Start Marketing Date: 20090324

Package Information of Cefazolin

Package NDC: 0409-0805-01
Package Description: 25 VIAL in 1 CARTON (0409-0805-01) > 3 mL in 1 VIAL

NDC Information of Cefazolin

NDC Code 0409-0805-01
Proprietary Name Cefazolin
Package Description 25 VIAL in 1 CARTON (0409-0805-01) > 3 mL in 1 VIAL
Product NDC 0409-0805
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cefazolin
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20090324
Marketing Category Name ANDA
Labeler Name Hospira, 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