NDC Code | 71288-009-20 |
Package Description | 10 VIAL, SINGLE-DOSE in 1 CARTON (71288-009-20) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (71288-009-21) |
Product NDC | 71288-009 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Cefepime |
Non-Proprietary Name | Cefepime Hydrochloride |
Dosage Form | INJECTION, POWDER, FOR SOLUTION |
Usage | INTRAVENOUS |
Start Marketing Date | 20181217 |
Marketing Category Name | ANDA |
Application Number | ANDA091048 |
Manufacturer | Meitheal Pharmaceuticals Inc. |
Substance Name | CEFEPIME HYDROCHLORIDE |
Strength | 2 |
Strength Unit | g/1 |
Pharmacy Classes | Cephalosporin Antibacterial [EPC], Cephalosporins [CS] |