| Product NDC: | 67684-1001 |
| Proprietary Name: | Oxilan |
| Non Proprietary Name: | Ioxilan Injection |
| Active Ingredient(s): | 350 mg/mL & nbsp; Ioxilan Injection |
| Administration Route(s): | INTRAVASCULAR |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 67684-1001 |
| Labeler Name: | Guerbet LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020316 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20020318 |
| Package NDC: | 67684-1001-5 |
| Package Description: | 6 BOTTLE in 1 CARTON (67684-1001-5) > 500 mL in 1 BOTTLE |
| NDC Code | 67684-1001-5 |
| Proprietary Name | Oxilan |
| Package Description | 6 BOTTLE in 1 CARTON (67684-1001-5) > 500 mL in 1 BOTTLE |
| Product NDC | 67684-1001 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ioxilan Injection |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVASCULAR |
| Start Marketing Date | 20020318 |
| Marketing Category Name | NDA |
| Labeler Name | Guerbet LLC |
| Substance Name | IOXILAN |
| Strength Number | 350 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Radiographic Contrast Agent [EPC],X-Ray Contrast Activity [MoA] |