Cefazolin - 55154-5439-5 - (Cefazolin)

Alphabetical Index


Drug Information of Cefazolin

Product NDC: 55154-5439
Proprietary Name: Cefazolin
Non Proprietary Name: Cefazolin
Active Ingredient(s): 1    g/1 & nbsp;   Cefazolin
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS; PARENTERAL
Dosage Form(s): INJECTION, POWDER, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Cefazolin

Product NDC: 55154-5439
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA062831
Marketing Category: ANDA
Start Marketing Date: 19881209

Package Information of Cefazolin

Package NDC: 55154-5439-5
Package Description: 5 VIAL in 1 BAG (55154-5439-5) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL

NDC Information of Cefazolin

NDC Code 55154-5439-5
Proprietary Name Cefazolin
Package Description 5 VIAL in 1 BAG (55154-5439-5) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
Product NDC 55154-5439
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cefazolin
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS; PARENTERAL
Start Marketing Date 19881209
Marketing Category Name ANDA
Labeler Name Cardinal Health
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