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 DescriptionPotassium 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:

Manufacturer / LabelerProprietary Name
American Regent, Inc.Potassium Acetate
Exela Pharma Sciences, LLC.Potassium Acetate
Hahnemann Laboratories, Inc.Kali Aceticum
Hospira, Inc.Potassium Acetate