Potassium Acetate (American Regent, Inc.)
Welcome to the PulseAid listing for the Potassium Acetate drug offered from American Regent, Inc.. This Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA] 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: | Potassium Acetate |
| SUBSTANCE NAME: | POTASSIUM ACETATE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA] |
| ROUTE: | INTRAVENOUS |
| DOSAGE FORM: | INJECTION, SOLUTION |
| MARKETING CATEGORY NAME: | UNAPPROVED DRUG OTHER |
| START MARKETING DATE: | 1990-09-30 |
| END MARKETING DATE: | 0000-00-00 |
Potassium Acetate HUMAN PRESCRIPTION DRUG Details:
| Item Description | Potassium Acetate from American Regent, Inc. |
| LABELER NAME: | American Regent, Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 196(mg/mL) |
| START MARKETING DATE: | 1990-09-30 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 0517-2053_85db0573-7200-41ba-9108-ba632c71dcca |
| PRODUCT NDC: | 0517-2053 |
| APPLICATION NUMBER: | |
Other POTASSIUM ACETATE Pharmaceutical Manufacturers / Labelers:
