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OMNIPAQUE
OMNIPAQUE - 0407-1412-29 - (Iohexol)
Drug Information of OMNIPAQUE
| Product NDC: | 0407-1412 |
| Proprietary Name: | OMNIPAQUE |
| Non Proprietary Name: | Iohexol |
| Active Ingredient(s): | 518 mg/mL & nbsp; Iohexol |
| Administration Route(s): | INTRATHECAL; INTRAVASCULAR; INTRAVENOUS; ORAL |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of OMNIPAQUE
| Product NDC: | 0407-1412 |
| Labeler Name: | GE Healthcare Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018956 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20050811 |
Package Information of OMNIPAQUE
| Package NDC: | 0407-1412-29 |
| Package Description: | 10 BOTTLE, PLASTIC in 1 BOX (0407-1412-29) > 50 mL in 1 BOTTLE, PLASTIC |
NDC Information of OMNIPAQUE
| NDC Code | 0407-1412-29 |
| Proprietary Name | OMNIPAQUE |
| Package Description | 10 BOTTLE, PLASTIC in 1 BOX (0407-1412-29) > 50 mL in 1 BOTTLE, PLASTIC |
| Product NDC | 0407-1412 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Iohexol |
| Dosage Form Name | INJECTION |
| Route Name | INTRATHECAL; INTRAVASCULAR; INTRAVENOUS; ORAL |
| Start Marketing Date | 20050811 |
| Marketing Category Name | NDA |
| Labeler Name | GE Healthcare Inc. |
| Substance Name | IOHEXOL |
| Strength Number | 518 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Radiographic Contrast Agent [EPC],X-Ray Contrast Activity [MoA] |
