CEFAZOLIN - 63323-236-10 - (CEFAZOLIN SODIUM)

Alphabetical Index


Drug Information of CEFAZOLIN

Product NDC: 63323-236
Proprietary Name: CEFAZOLIN
Non Proprietary Name: CEFAZOLIN SODIUM
Active Ingredient(s): 500    mg/2.2mL & nbsp;   CEFAZOLIN SODIUM
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): POWDER, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of CEFAZOLIN

Product NDC: 63323-236
Labeler Name: APP Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065303
Marketing Category: ANDA
Start Marketing Date: 20110715

Package Information of CEFAZOLIN

Package NDC: 63323-236-10
Package Description: 25 VIAL in 1 CARTON (63323-236-10) > 2.2 mL in 1 VIAL

NDC Information of CEFAZOLIN

NDC Code 63323-236-10
Proprietary Name CEFAZOLIN
Package Description 25 VIAL in 1 CARTON (63323-236-10) > 2.2 mL in 1 VIAL
Product NDC 63323-236
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CEFAZOLIN SODIUM
Dosage Form Name POWDER, FOR SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20110715
Marketing Category Name ANDA
Labeler Name APP Pharmaceuticals, LLC
Substance Name CEFAZOLIN SODIUM
Strength Number 500
Strength Unit mg/2.2mL
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of CEFAZOLIN


General Information