Product NDC: | 0019-0952 |
Proprietary Name: | Conray 30 |
Non Proprietary Name: | Iothalamate Meglumine |
Active Ingredient(s): | 300 mg/mL & nbsp; Iothalamate Meglumine |
Administration Route(s): | INTRAVASCULAR |
Dosage Form(s): | INJECTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0019-0952 |
Labeler Name: | Mallinckrodt Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA016983 |
Marketing Category: | NDA |
Start Marketing Date: | 20120326 |
Package NDC: | 0019-0952-15 |
Package Description: | 50 VIAL, GLASS in 1 BOX (0019-0952-15) > 50 mL in 1 VIAL, GLASS |
NDC Code | 0019-0952-15 |
Proprietary Name | Conray 30 |
Package Description | 50 VIAL, GLASS in 1 BOX (0019-0952-15) > 50 mL in 1 VIAL, GLASS |
Product NDC | 0019-0952 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Iothalamate Meglumine |
Dosage Form Name | INJECTION |
Route Name | INTRAVASCULAR |
Start Marketing Date | 20120326 |
Marketing Category Name | NDA |
Labeler Name | Mallinckrodt Inc. |
Substance Name | IOTHALAMATE MEGLUMINE |
Strength Number | 300 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Radiographic Contrast Agent [EPC],X-Ray Contrast Activity [MoA] |