Cefazolin - 66288-1100-1 - (Cefazolin Sodium)

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Drug Information of Cefazolin

Product NDC: 66288-1100
Proprietary Name: Cefazolin
Non Proprietary Name: Cefazolin Sodium
Active Ingredient(s): 100    g/1 & nbsp;   Cefazolin Sodium
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Cefazolin

Product NDC: 66288-1100
Labeler Name: Samson Medical Technologies, L.L.C.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065141
Marketing Category: ANDA
Start Marketing Date: 20070101

Package Information of Cefazolin

Package NDC: 66288-1100-1
Package Description: 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 BAG (66288-1100-1)

NDC Information of Cefazolin

NDC Code 66288-1100-1
Proprietary Name Cefazolin
Package Description 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 BAG (66288-1100-1)
Product NDC 66288-1100
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cefazolin Sodium
Dosage Form Name INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20070101
Marketing Category Name ANDA
Labeler Name Samson Medical Technologies, L.L.C.
Substance Name CEFAZOLIN SODIUM
Strength Number 100
Strength Unit g/1
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of Cefazolin


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