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 |