NDC 51754-2001
Potassium Acetate
Potassium Acetate
Potassium Acetate is a Intravenous Injection, Solution, Concentrate in the Human Prescription Drug category. It is labeled and distributed by Exela Pharma Sciences, Llc.. The primary component is Potassium Acetate.
| Product ID | 51754-2001_7d02042f-8453-43f3-b920-29bb1283fc1b |
| NDC | 51754-2001 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Potassium Acetate |
| Generic Name | Potassium Acetate |
| Dosage Form | Injection, Solution, Concentrate |
| Route of Administration | INTRAVENOUS |
| Marketing Start Date | 2016-01-07 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA206203 |
| Labeler Name | Exela Pharma Sciences, LLC. |
| Substance Name | POTASSIUM ACETATE |
| Active Ingredient Strength | 4 g/20mL |
| Pharm Classes | Potassium Compounds [CS],Potassium Salt [EPC],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2021-12-31 |