| Product NDC: | 0703-4116 |
| Proprietary Name: | Ifosfamide and Mesna |
| Non Proprietary Name: | Ifosfamide and Mesna |
| Active Ingredient(s): | & nbsp; Ifosfamide and Mesna |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0703-4116 |
| Labeler Name: | Teva Parenteral Medicines, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075874 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120926 |
| Package NDC: | 0703-4116-48 |
| Package Description: | 1 KIT in 1 CARTON (0703-4116-48) * 20 mL in 1 VIAL, SINGLE-DOSE (0703-3407-01) * 10 mL in 1 VIAL, MULTI-DOSE (0703-4805-01) |
| NDC Code | 0703-4116-48 |
| Proprietary Name | Ifosfamide and Mesna |
| Package Description | 1 KIT in 1 CARTON (0703-4116-48) * 20 mL in 1 VIAL, SINGLE-DOSE (0703-3407-01) * 10 mL in 1 VIAL, MULTI-DOSE (0703-4805-01) |
| Product NDC | 0703-4116 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ifosfamide and Mesna |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20120926 |
| Marketing Category Name | ANDA |
| Labeler Name | Teva Parenteral Medicines, Inc |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |