Home
>
National Drug Code (NDC)
>
Cefazolin
Cefazolin - 0781-3450-95 - (Cefazolin)
Drug Information of Cefazolin
| Product NDC: | 0781-3450 |
| Proprietary Name: | Cefazolin |
| Non Proprietary Name: | Cefazolin |
| Active Ingredient(s): | 500 mg/1 & nbsp; Cefazolin |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS; PARENTERAL |
| Dosage Form(s): | INJECTION, POWDER, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cefazolin
| Product NDC: | 0781-3450 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA062831 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19881209 |
Package Information of Cefazolin
| Package NDC: | 0781-3450-95 |
| Package Description: | 10 VIAL in 1 CARTON (0781-3450-95) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0781-3450-70) |
NDC Information of Cefazolin
| NDC Code | 0781-3450-95 |
| Proprietary Name | Cefazolin |
| Package Description | 10 VIAL in 1 CARTON (0781-3450-95) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0781-3450-70) |
| Product NDC | 0781-3450 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Cefazolin |
| Dosage Form Name | INJECTION, POWDER, FOR SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS; PARENTERAL |
| Start Marketing Date | 19881209 |
| Marketing Category Name | ANDA |
| Labeler Name | Sandoz Inc |
| Substance Name | CEFAZOLIN SODIUM |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] |
