Selenium (American Regent, Inc.)
Welcome to the PulseAid listing for the Selenium drug offered from American Regent, Inc.. 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: | American Regent, Inc. |
| NON-PROPRIETARY NAME: | Selenium |
| SUBSTANCE NAME: | SELENIOUS ACID |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | |
| ROUTE: | INTRAVENOUS |
| DOSAGE FORM: | INJECTION, SOLUTION |
| MARKETING CATEGORY NAME: | UNAPPROVED DRUG OTHER |
| START MARKETING DATE: | 1990-09-30 |
| END MARKETING DATE: | 0000-00-00 |
Selenium HUMAN PRESCRIPTION DRUG Details:
| Item Description | Selenium from American Regent, Inc. |
| LABELER NAME: | American Regent, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 65.4(ug/mL) |
| START MARKETING DATE: | 1990-09-30 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0517-6510_51f40bae-9b0e-4937-8f15-4e3e8dbeddd0 |
| PRODUCT NDC: | 0517-6510 |
| APPLICATION NUMBER: | |
Other SELENIOUS ACID Pharmaceutical Manufacturers / Labelers:
