Product NDC: | 0270-1317 |
Proprietary Name: | Isovue |
Non Proprietary Name: | IOPAMIDOL |
Active Ingredient(s): | 510 mg/mL & nbsp; IOPAMIDOL |
Administration Route(s): | INTRAVASCULAR |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0270-1317 |
Labeler Name: | Bracco Diagnostics Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA018735 |
Marketing Category: | NDA |
Start Marketing Date: | 19941012 |
Package NDC: | 0270-1317-05 |
Package Description: | 10 VIAL, SINGLE-DOSE in 1 BOX (0270-1317-05) > 50 mL in 1 VIAL, SINGLE-DOSE |
NDC Code | 0270-1317-05 |
Proprietary Name | Isovue |
Package Description | 10 VIAL, SINGLE-DOSE in 1 BOX (0270-1317-05) > 50 mL in 1 VIAL, SINGLE-DOSE |
Product NDC | 0270-1317 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | IOPAMIDOL |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVASCULAR |
Start Marketing Date | 19941012 |
Marketing Category Name | NDA |
Labeler Name | Bracco Diagnostics Inc |
Substance Name | IOPAMIDOL |
Strength Number | 510 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Radiographic Contrast Agent [EPC],X-Ray Contrast Activity [MoA] |