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] |