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HICON
HICON - 65174-880-50 - (Sodium Iodide I 131)
Drug Information of HICON
| Product NDC: | 65174-880 |
| Proprietary Name: | HICON |
| Non Proprietary Name: | Sodium Iodide I 131 |
| Active Ingredient(s): | 1 mCi/mL & nbsp; Sodium Iodide I 131 |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of HICON
| Product NDC: | 65174-880 |
| Labeler Name: | Jubilant DraxImage Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021305 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20030407 |
Package Information of HICON
| Package NDC: | 65174-880-50 |
| Package Description: | 1 VIAL in 1 KIT (65174-880-50) > .5 mL in 1 VIAL |
NDC Information of HICON
| NDC Code | 65174-880-50 |
| Proprietary Name | HICON |
| Package Description | 1 VIAL in 1 KIT (65174-880-50) > .5 mL in 1 VIAL |
| Product NDC | 65174-880 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sodium Iodide I 131 |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20030407 |
| Marketing Category Name | NDA |
| Labeler Name | Jubilant DraxImage Inc. |
| Substance Name | SODIUM IODIDE I-131 |
| Strength Number | 1 |
| Strength Unit | mCi/mL |
| Pharmaceutical Classes |
