Product NDC: | 0143-9768 |
Proprietary Name: | Ceftriaxone |
Non Proprietary Name: | Ceftriaxone |
Active Ingredient(s): | 10 g/100mL & nbsp; Ceftriaxone |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | POWDER, FOR SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0143-9768 |
Labeler Name: | West-ward Pharmaceutical Corp |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA065328 |
Marketing Category: | NDA |
Start Marketing Date: | 20090806 |
Package NDC: | 0143-9768-46 |
Package Description: | 1 VIAL in 1 BOX (0143-9768-46) > 100 mL in 1 VIAL (0143-9768-01) |
NDC Code | 0143-9768-46 |
Proprietary Name | Ceftriaxone |
Package Description | 1 VIAL in 1 BOX (0143-9768-46) > 100 mL in 1 VIAL (0143-9768-01) |
Product NDC | 0143-9768 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Ceftriaxone |
Dosage Form Name | POWDER, FOR SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20090806 |
Marketing Category Name | NDA |
Labeler Name | West-ward Pharmaceutical Corp |
Substance Name | CEFTRIAXONE SODIUM |
Strength Number | 10 |
Strength Unit | g/100mL |
Pharmaceutical Classes | Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] |