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Isovue
Isovue - 0270-1317-41 - (IOPAMIDOL)
Drug Information of Isovue
| 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) |
Labeler Information of Isovue
| 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 Information of Isovue
| Package NDC: | 0270-1317-41 |
| Package Description: | 10 BOTTLE in 1 BOX (0270-1317-41) > 200 mL in 1 BOTTLE |
NDC Information of Isovue
| NDC Code | 0270-1317-41 |
| Proprietary Name | Isovue |
| Package Description | 10 BOTTLE in 1 BOX (0270-1317-41) > 200 mL in 1 BOTTLE |
| 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] |
