Potassium Acetate (Exela Pharma Sciences, LLC.)
Welcome to the PulseAid listing for the Potassium Acetate drug offered from Exela Pharma Sciences, LLC.. 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: | Exela Pharma Sciences, LLC. |
| 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, CONCENTRATE |
| MARKETING CATEGORY NAME: | ANDA |
| START MARKETING DATE: | 2016-01-07 |
| END MARKETING DATE: | 0000-00-00 |
Potassium Acetate HUMAN PRESCRIPTION DRUG Details:
| Item Description | Potassium Acetate from Exela Pharma Sciences, LLC. |
| LABELER NAME: | Exela Pharma Sciences, LLC. |
| DEA SCHEDULE: |
|
| ACTIVE STRENGTH: | 3.93(g/20mL) |
| START MARKETING DATE: | 2016-01-07 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 51754-2001_c71cf751-42a9-4fb0-a43d-edfb68ad9c85 |
| PRODUCT NDC: | 51754-2001 |
| APPLICATION NUMBER: | ANDA206203 |
Other POTASSIUM ACETATE Pharmaceutical Manufacturers / Labelers:
