| Product NDC: | 0270-1314 |
| Proprietary Name: | Isovue |
| Non Proprietary Name: | IOPAMIDOL |
| Active Ingredient(s): | 408 mg/mL & nbsp; IOPAMIDOL |
| Administration Route(s): | INTRAVASCULAR |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0270-1314 |
| Labeler Name: | Bracco Diagnostics Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018735 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19941012 |
| Package NDC: | 0270-1314-30 |
| Package Description: | 10 VIAL, SINGLE-DOSE in 1 BOX (0270-1314-30) > 50 mL in 1 VIAL, SINGLE-DOSE |
| NDC Code | 0270-1314-30 |
| Proprietary Name | Isovue |
| Package Description | 10 VIAL, SINGLE-DOSE in 1 BOX (0270-1314-30) > 50 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 0270-1314 |
| 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 | 408 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Radiographic Contrast Agent [EPC],X-Ray Contrast Activity [MoA] |