Cefazolin - 63323-446-66 - (Cefazolin)

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Drug Information of Cefazolin

Product NDC: 63323-446
Proprietary Name: Cefazolin
Non Proprietary Name: Cefazolin
Active Ingredient(s): 20    g/100mL & 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: 63323-446
Labeler Name: APP Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA063209
Marketing Category: ANDA
Start Marketing Date: 20120713

Package Information of Cefazolin

Package NDC: 63323-446-66
Package Description: 10 VIAL in 1 CARTON (63323-446-66) > 100 mL in 1 VIAL

NDC Information of Cefazolin

NDC Code 63323-446-66
Proprietary Name Cefazolin
Package Description 10 VIAL in 1 CARTON (63323-446-66) > 100 mL in 1 VIAL
Product NDC 63323-446
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cefazolin
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20120713
Marketing Category Name ANDA
Labeler Name APP Pharmaceuticals, LLC
Substance Name CEFAZOLIN SODIUM
Strength Number 20
Strength Unit g/100mL
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of Cefazolin


General Information