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] |