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Ifosfamide
Ifosfamide - 55390-048-01 - (Ifosfamide)
Drug Information of Ifosfamide
| Product NDC: | 55390-048 |
| Proprietary Name: | Ifosfamide |
| Non Proprietary Name: | Ifosfamide |
| Active Ingredient(s): | 50 mg/mL & nbsp; Ifosfamide |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ifosfamide
| Product NDC: | 55390-048 |
| Labeler Name: | Bedford Laboratories |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076619 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100831 |
Package Information of Ifosfamide
| Package NDC: | 55390-048-01 |
| Package Description: | 1 VIAL, SINGLE-DOSE in 1 BOX (55390-048-01) > 60 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of Ifosfamide
| NDC Code | 55390-048-01 |
| Proprietary Name | Ifosfamide |
| Package Description | 1 VIAL, SINGLE-DOSE in 1 BOX (55390-048-01) > 60 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 55390-048 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ifosfamide |
| Dosage Form Name | INJECTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20100831 |
| Marketing Category Name | ANDA |
| Labeler Name | Bedford Laboratories |
| Substance Name | IFOSFAMIDE |
| Strength Number | 50 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Alkylating Activity [MoA],Alkylating Drug [EPC] |
