NDC 51754-9995
Sodium Acetate
Sodium Acetate
Sodium Acetate is a Intravenous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Exela Pharma Sciences, Llc. The primary component is Sodium Acetate Anhydrous.
| Product ID | 51754-9995_e11ab1a1-8cc7-4d3b-ad29-af4c9aaa3ed4 |
| NDC | 51754-9995 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Sodium Acetate |
| Generic Name | Sodium Acetate |
| Dosage Form | Injection, Solution |
| Route of Administration | INTRAVENOUS |
| Marketing Start Date | 2022-07-01 |
| Marketing Category | UNAPPROVED DRUG OTHER / |
| Labeler Name | Exela Pharma Sciences, LLC |
| Substance Name | SODIUM ACETATE ANHYDROUS |
| Active Ingredient Strength | 200 meq/100mL |
| Pharm Classes | Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2023-12-31 |