| Product NDC: | 54868-4651 | 
| Proprietary Name: | Cefazolin | 
| Non Proprietary Name: | Cefazolin sodium | 
| Active Ingredient(s): | 500 mg/10mL & nbsp; Cefazolin sodium | 
| Administration Route(s): | INTRAMUSCULAR | 
| Dosage Form(s): | INJECTION | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 54868-4651 | 
| Labeler Name: | Physicians Total Care, Inc. | 
| Product Type: | HUMAN PRESCRIPTION DRUG | 
| FDA Application Number: | ANDA065047 | 
| Marketing Category: | ANDA | 
| Start Marketing Date: | 20030915 | 
| Package NDC: | 54868-4651-0 | 
| Package Description: | 25 VIAL in 1 CARTON (54868-4651-0) > 10 mL in 1 VIAL | 
| NDC Code | 54868-4651-0 | 
| Proprietary Name | Cefazolin | 
| Package Description | 25 VIAL in 1 CARTON (54868-4651-0) > 10 mL in 1 VIAL | 
| Product NDC | 54868-4651 | 
| Product Type Name | HUMAN PRESCRIPTION DRUG | 
| Non Proprietary Name | Cefazolin sodium | 
| Dosage Form Name | INJECTION | 
| Route Name | INTRAMUSCULAR | 
| Start Marketing Date | 20030915 | 
| Marketing Category Name | ANDA | 
| Labeler Name | Physicians Total Care, Inc. | 
| Substance Name | CEFAZOLIN SODIUM | 
| Strength Number | 500 | 
| Strength Unit | mg/10mL | 
| Pharmaceutical Classes | Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] |