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Ifosfamide
Ifosfamide - 63323-174-20 - (IFOSFAMIDE)
Drug Information of Ifosfamide
| Product NDC: | 63323-174 |
| Proprietary Name: | Ifosfamide |
| Non Proprietary Name: | IFOSFAMIDE |
| Active Ingredient(s): | 50 mg/mL & nbsp; IFOSFAMIDE |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ifosfamide
| Product NDC: | 63323-174 |
| Labeler Name: | APP Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090181 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090930 |
Package Information of Ifosfamide
| Package NDC: | 63323-174-20 |
| Package Description: | 1 VIAL, SINGLE-DOSE in 1 CARTON (63323-174-20) > 20 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of Ifosfamide
| NDC Code | 63323-174-20 |
| Proprietary Name | Ifosfamide |
| Package Description | 1 VIAL, SINGLE-DOSE in 1 CARTON (63323-174-20) > 20 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 63323-174 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | IFOSFAMIDE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20090930 |
| Marketing Category Name | ANDA |
| Labeler Name | APP Pharmaceuticals, LLC |
| Substance Name | IFOSFAMIDE |
| Strength Number | 50 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Alkylating Activity [MoA],Alkylating Drug [EPC] |
