Sodum Acetate (American Regent, Inc.)
Welcome to the PulseAid listing for the Sodum Acetate 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: | Sodium Acetate |
| SUBSTANCE NAME: | SODIUM ACETATE ANHYDROUS |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | |
| ROUTE: | INTRAVENOUS |
| DOSAGE FORM: | INJECTION, SOLUTION, CONCENTRATE |
| MARKETING CATEGORY NAME: | UNAPPROVED DRUG OTHER |
| START MARKETING DATE: | 1990-09-30 |
| END MARKETING DATE: | 0000-00-00 |
Sodum Acetate HUMAN PRESCRIPTION DRUG Details:
| Item Description | Sodum Acetate from American Regent, Inc. |
| LABELER NAME: | American Regent, Inc. |
| DEA SCHEDULE: |
|
| ACTIVE STRENGTH: | 328(mg/mL) |
| START MARKETING DATE: | 1990-09-30 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0517-5023_0954629f-ef6f-42d1-b3c9-409597fb8a24 |
| PRODUCT NDC: | 0517-5023 |
| APPLICATION NUMBER: | |
Other SODIUM ACETATE ANHYDROUS Pharmaceutical Manufacturers / Labelers:
