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OMNIPAQUE
OMNIPAQUE - 0407-1414-87 - (Iohexol)
Drug Information of OMNIPAQUE
| Product NDC: | 0407-1414 |
| Proprietary Name: | OMNIPAQUE |
| Non Proprietary Name: | Iohexol |
| Active Ingredient(s): | 755 mg/mL & nbsp; Iohexol |
| Administration Route(s): | INTRAVASCULAR; INTRAVENOUS; ORAL |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of OMNIPAQUE
| Product NDC: | 0407-1414 |
| Labeler Name: | GE Healthcare Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018956 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20060721 |
Package Information of OMNIPAQUE
| Package NDC: | 0407-1414-87 |
| Package Description: | 10 BOTTLE, PLASTIC in 1 BOX (0407-1414-87) > 200 mL in 1 BOTTLE, PLASTIC |
NDC Information of OMNIPAQUE
| NDC Code | 0407-1414-87 |
| Proprietary Name | OMNIPAQUE |
| Package Description | 10 BOTTLE, PLASTIC in 1 BOX (0407-1414-87) > 200 mL in 1 BOTTLE, PLASTIC |
| Product NDC | 0407-1414 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Iohexol |
| Dosage Form Name | INJECTION |
| Route Name | INTRAVASCULAR; INTRAVENOUS; ORAL |
| Start Marketing Date | 20060721 |
| Marketing Category Name | NDA |
| Labeler Name | GE Healthcare Inc. |
| Substance Name | IOHEXOL |
| Strength Number | 755 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Radiographic Contrast Agent [EPC],X-Ray Contrast Activity [MoA] |
