| Product NDC: | 52533-015 | 
| Proprietary Name: | Cefazolin Sodium | 
| Non Proprietary Name: | Cefazolin Sodium | 
| Active Ingredient(s): | 2 g/100mL & nbsp; Cefazolin Sodium | 
| Administration Route(s): | INTRAVENOUS | 
| Dosage Form(s): | INJECTION, SOLUTION | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 52533-015 | 
| Labeler Name: | Cantrell Drug Company | 
| Product Type: | HUMAN PRESCRIPTION DRUG | 
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER | 
| Start Marketing Date: | 20110930 | 
| Package NDC: | 52533-015-14 | 
| Package Description: | 100 mL in 1 BAG (52533-015-14) | 
| NDC Code | 52533-015-14 | 
| Proprietary Name | Cefazolin Sodium | 
| Package Description | 100 mL in 1 BAG (52533-015-14) | 
| Product NDC | 52533-015 | 
| Product Type Name | HUMAN PRESCRIPTION DRUG | 
| Non Proprietary Name | Cefazolin Sodium | 
| Dosage Form Name | INJECTION, SOLUTION | 
| Route Name | INTRAVENOUS | 
| Start Marketing Date | 20110930 | 
| Marketing Category Name | UNAPPROVED DRUG OTHER | 
| Labeler Name | Cantrell Drug Company | 
| Substance Name | CEFAZOLIN SODIUM | 
| Strength Number | 2 | 
| Strength Unit | g/100mL | 
| Pharmaceutical Classes | Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] |