| NDC Code | 63323-142-12 |
|---|
| Package Description | 1 VIAL, SINGLE-DOSE in 1 BOX (63323-142-12) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-DOSE |
|---|
| Product NDC | 63323-142 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Ifosfamide |
|---|
| Non-Proprietary Name | Ifosfamide |
|---|
| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
|---|
| Usage | INTRAVENOUS |
|---|
| Start Marketing Date | 20030128 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA076078 |
|---|
| Manufacturer | Fresenius Kabi USA, LLC |
|---|
| Substance Name | IFOSFAMIDE |
|---|
| Strength | 1 |
|---|
| Strength Unit | g/1 |
|---|
| Pharmacy Classes | Alkylating Activity [MoA], Alkylating Drug [EPC] |
|---|