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Conray
Conray - 0019-0953-13 - (iothalamate meglumine)
Drug Information of Conray
| Product NDC: | 0019-0953 |
| Proprietary Name: | Conray |
| Non Proprietary Name: | iothalamate meglumine |
| Active Ingredient(s): | 600 mg/mL & nbsp; iothalamate meglumine |
| Administration Route(s): | INTRAVASCULAR |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Conray
| Product NDC: | 0019-0953 |
| Labeler Name: | Mallinckrodt Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA013295 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20031014 |
Package Information of Conray
| Package NDC: | 0019-0953-13 |
| Package Description: | 50 VIAL, GLASS in 1 BOX (0019-0953-13) > 30 mL in 1 VIAL, GLASS |
NDC Information of Conray
| NDC Code | 0019-0953-13 |
| Proprietary Name | Conray |
| Package Description | 50 VIAL, GLASS in 1 BOX (0019-0953-13) > 30 mL in 1 VIAL, GLASS |
| Product NDC | 0019-0953 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | iothalamate meglumine |
| Dosage Form Name | INJECTION |
| Route Name | INTRAVASCULAR |
| Start Marketing Date | 20031014 |
| Marketing Category Name | NDA |
| Labeler Name | Mallinckrodt Inc. |
| Substance Name | IOTHALAMATE MEGLUMINE |
| Strength Number | 600 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Radiographic Contrast Agent [EPC],X-Ray Contrast Activity [MoA] |
