Product NDC: | 67684-1000 |
Proprietary Name: | Oxilan |
Non Proprietary Name: | Ioxilan Injection |
Active Ingredient(s): | 300 mg/mL & nbsp; Ioxilan Injection |
Administration Route(s): | INTRAVASCULAR |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 67684-1000 |
Labeler Name: | Guerbet LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020316 |
Marketing Category: | NDA |
Start Marketing Date: | 20020318 |
Package NDC: | 67684-1000-5 |
Package Description: | 6 BOTTLE in 1 CARTON (67684-1000-5) > 500 mL in 1 BOTTLE |
NDC Code | 67684-1000-5 |
Proprietary Name | Oxilan |
Package Description | 6 BOTTLE in 1 CARTON (67684-1000-5) > 500 mL in 1 BOTTLE |
Product NDC | 67684-1000 |
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 | 300 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Radiographic Contrast Agent [EPC],X-Ray Contrast Activity [MoA] |