Plasma-Lyte A is a Intravenous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Baxter Healthcare Corporation. The primary component is Sodium Chloride; Sodium Gluconate; Sodium Acetate; Potassium Chloride; Magnesium Chloride.
| Product ID | 0338-0221_3b95c0b2-4879-4af4-9319-a1a0ceb103f3 |
| NDC | 0338-0221 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Plasma-Lyte A |
| Generic Name | Sodium Chloride, Sodium Gluconate, Sodium Acetate, Potassium Chloride And Magnesium Chloride |
| Dosage Form | Injection, Solution |
| Route of Administration | INTRAVENOUS |
| Marketing Start Date | 1979-02-02 |
| Marketing Category | NDA / NDA |
| Application Number | NDA017378 |
| Labeler Name | Baxter Healthcare Corporation |
| Substance Name | SODIUM CHLORIDE; SODIUM GLUCONATE; SODIUM ACETATE; POTASSIUM CHLORIDE; MAGNESIUM CHLORIDE |
| Active Ingredient Strength | 526 mg/100mL; mg/100mL; mg/100mL; mg/100mL; mg/100mL |
| Pharm Classes | Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA],Potassium Compounds [CS],Potassium Salt [EPC],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA],Calculi Dissolution Agent [EPC],Magnesium Ion Exchange Activity [MoA],Osmotic Laxative [EPC],Osmotic Activity [MoA],Inhibition Small Intestine Fluid/Electrolyte Absorption [PE],Increased Large Intestinal Motility [PE],Stimulation Large Intestine Fluid/Electrolyte Secretion [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2020-12-31 |
| Marketing Start Date | 1979-02-02 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | NDA |
| Application Number | NDA017378 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 1979-02-02 |
| Marketing Category | NDA |
| Application Number | NDA017378 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 1979-02-02 |
| Ingredient | Strength |
|---|---|
| SODIUM CHLORIDE | 526 mg/100mL |
| SPL SET ID: | 6ec9e61c-2c26-402f-8604-f446b2e34058 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0338-0221 | Plasma-Lyte A | Sodium Chloride, Sodium Gluconate, Sodium Acetate, Potassium Chloride and Magnesium Chloride |
| 65219-387 | Multiple Electrolytes pH 5.5 | sodium chloride, sodium gluconate, sodium acetate, potassium chloride and magnesium chloride |
| 65219-389 | Multiple Electrolytes pH 7.4 | sodium chloride, sodium gluconate, sodium acetate, potassium chloride and magnesium chloride |