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IFEX
IFEX - 0338-3991-01 - (ifosfamide)
Drug Information of IFEX
| Product NDC: | 0338-3991 |
| Proprietary Name: | IFEX |
| Non Proprietary Name: | ifosfamide |
| Active Ingredient(s): | 1 g/1 & nbsp; ifosfamide |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of IFEX
| Product NDC: | 0338-3991 |
| Labeler Name: | BAXTER HEALTHCARE CORPORATION |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019763 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20120301 |
Package Information of IFEX
| Package NDC: | 0338-3991-01 |
| Package Description: | 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (0338-3991-01) |
NDC Information of IFEX
| NDC Code | 0338-3991-01 |
| Proprietary Name | IFEX |
| Package Description | 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (0338-3991-01) |
| Product NDC | 0338-3991 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ifosfamide |
| Dosage Form Name | INJECTION, POWDER, FOR SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20120301 |
| Marketing Category Name | NDA |
| Labeler Name | BAXTER HEALTHCARE CORPORATION |
| Substance Name | IFOSFAMIDE |
| Strength Number | 1 |
| Strength Unit | g/1 |
| Pharmaceutical Classes | Alkylating Activity [MoA],Alkylating Drug [EPC] |
