Iodopen Sodium Iodide (APP Pharmaceuticals, LLC)
Welcome to the PulseAid listing for the Iodopen Sodium Iodide drug offered from APP Pharmaceuticals, LLC. This pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
| LABELER NAME / MANUFACTURER: | APP Pharmaceuticals, LLC |
| NON-PROPRIETARY NAME: | SODIUM IODIDE |
| SUBSTANCE NAME: | SODIUM IODIDE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | |
| ROUTE: | INTRAVENOUS |
| DOSAGE FORM: | INJECTION, SOLUTION |
| MARKETING CATEGORY NAME: | UNAPPROVED DRUG OTHER |
| START MARKETING DATE: | 2001-07-18 |
| END MARKETING DATE: | 0000-00-00 |
Iodopen Sodium Iodide HUMAN PRESCRIPTION DRUG Details:
| Item Description | Iodopen Sodium Iodide from APP Pharmaceuticals, LLC |
| LABELER NAME: | APP Pharmaceuticals, LLC |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 118(ug/mL) |
| START MARKETING DATE: | 2001-07-18 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 63323-019_ff54b240-853e-4fb6-9b9e-b52404f5f9eb |
| PRODUCT NDC: | 63323-019 |
| APPLICATION NUMBER: | |
Other SODIUM IODIDE Pharmaceutical Manufacturers / Labelers:
