Home
>
National Drug Code (NDC)
>
Ultravist
Ultravist - 50419-340-05 - (iopromide)
Drug Information of Ultravist
| Product NDC: | 50419-340 |
| Proprietary Name: | Ultravist |
| Non Proprietary Name: | iopromide |
| Active Ingredient(s): | 311.7 mg/mL & nbsp; iopromide |
| Administration Route(s): | INTRA-ARTERIAL; INTRAVENOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ultravist
| Product NDC: | 50419-340 |
| Labeler Name: | Bayer HealthCare Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020220 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20091230 |
Package Information of Ultravist
| Package NDC: | 50419-340-05 |
| Package Description: | 10 VIAL, GLASS in 1 CARTON (50419-340-05) > 50 mL in 1 VIAL, GLASS |
NDC Information of Ultravist
| NDC Code | 50419-340-05 |
| Proprietary Name | Ultravist |
| Package Description | 10 VIAL, GLASS in 1 CARTON (50419-340-05) > 50 mL in 1 VIAL, GLASS |
| Product NDC | 50419-340 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | iopromide |
| Dosage Form Name | INJECTION |
| Route Name | INTRA-ARTERIAL; INTRAVENOUS |
| Start Marketing Date | 20091230 |
| Marketing Category Name | NDA |
| Labeler Name | Bayer HealthCare Pharmaceuticals Inc. |
| Substance Name | IOPROMIDE |
| Strength Number | 311.7 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Radiographic Contrast Agent [EPC],X-Ray Contrast Activity [MoA] |
