Cefazolin - 0781-3452-95 - (Cefazolin)

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Drug Information of Cefazolin

Product NDC: 0781-3452
Proprietary Name: Cefazolin
Non Proprietary Name: Cefazolin
Active Ingredient(s): 10    g/1 & nbsp;   Cefazolin
Administration Route(s): INTRAVENOUS; PARENTERAL
Dosage Form(s): INJECTION, POWDER, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Cefazolin

Product NDC: 0781-3452
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA062831
Marketing Category: ANDA
Start Marketing Date: 19881209

Package Information of Cefazolin

Package NDC: 0781-3452-95
Package Description: 10 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (0781-3452-95) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, PHARMACY BULK PACKAGE (0781-3452-46)

NDC Information of Cefazolin

NDC Code 0781-3452-95
Proprietary Name Cefazolin
Package Description 10 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (0781-3452-95) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, PHARMACY BULK PACKAGE (0781-3452-46)
Product NDC 0781-3452
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cefazolin
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAVENOUS; PARENTERAL
Start Marketing Date 19881209
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name CEFAZOLIN SODIUM
Strength Number 10
Strength Unit g/1
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of Cefazolin


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