Product NDC: | 0019-3183 |
Proprietary Name: | Conray 43 |
Non Proprietary Name: | iothalamate meglumine |
Active Ingredient(s): | 430 mg/mL & nbsp; iothalamate meglumine |
Administration Route(s): | INTRAVASCULAR |
Dosage Form(s): | INJECTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0019-3183 |
Labeler Name: | Mallinckrodt Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA013295 |
Marketing Category: | NDA |
Start Marketing Date: | 20101011 |
Package NDC: | 0019-3183-11 |
Package Description: | 12 BOTTLE, GLASS in 1 BOX (0019-3183-11) > 200 mL in 1 BOTTLE, GLASS |
NDC Code | 0019-3183-11 |
Proprietary Name | Conray 43 |
Package Description | 12 BOTTLE, GLASS in 1 BOX (0019-3183-11) > 200 mL in 1 BOTTLE, GLASS |
Product NDC | 0019-3183 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | iothalamate meglumine |
Dosage Form Name | INJECTION |
Route Name | INTRAVASCULAR |
Start Marketing Date | 20101011 |
Marketing Category Name | NDA |
Labeler Name | Mallinckrodt Inc. |
Substance Name | IOTHALAMATE MEGLUMINE |
Strength Number | 430 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Radiographic Contrast Agent [EPC],X-Ray Contrast Activity [MoA] |