NDC Code | 70594-090-02 |
Package Description | 10 VIAL in 1 CARTON (70594-090-02) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (70594-090-01) |
Product NDC | 70594-090 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Cefepime Hydrochloride |
Non-Proprietary Name | Cefepime Hydrochloride |
Dosage Form | INJECTION, POWDER, FOR SOLUTION |
Usage | INTRAMUSCULAR; INTRAVENOUS |
Start Marketing Date | 20210110 |
Marketing Category Name | ANDA |
Application Number | ANDA212721 |
Manufacturer | Xellia Pharmaceuticals USA LLC |
Substance Name | CEFEPIME HYDROCHLORIDE |
Strength | 2 |
Strength Unit | g/1 |
Pharmacy Classes | Cephalosporin Antibacterial [EPC], Cephalosporins [CS] |