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: |
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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: