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Iodopen Sodium Iodide
Iodopen Sodium Iodide - 63323-019-10 - (SODIUM IODIDE)
Drug Information of Iodopen Sodium Iodide
| Product NDC: | 63323-019 |
| Proprietary Name: | Iodopen Sodium Iodide |
| Non Proprietary Name: | SODIUM IODIDE |
| Active Ingredient(s): | 118 ug/mL & nbsp; SODIUM IODIDE |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Iodopen Sodium Iodide
| Product NDC: | 63323-019 |
| Labeler Name: | APP Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20010718 |
Package Information of Iodopen Sodium Iodide
| Package NDC: | 63323-019-10 |
| Package Description: | 25 VIAL, SINGLE-DOSE in 1 TRAY (63323-019-10) > 10 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of Iodopen Sodium Iodide
| NDC Code | 63323-019-10 |
| Proprietary Name | Iodopen Sodium Iodide |
| Package Description | 25 VIAL, SINGLE-DOSE in 1 TRAY (63323-019-10) > 10 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 63323-019 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | SODIUM IODIDE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20010718 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | APP Pharmaceuticals, LLC |
| Substance Name | SODIUM IODIDE |
| Strength Number | 118 |
| Strength Unit | ug/mL |
| Pharmaceutical Classes |
