Plasma-Lyte A 30 mg/100mL
Sodium Chloride, Sodium Gluconate, Sodium Acetate, Potassium Chloride and Magnesium Chloride · INJECTION, SOLUTION · Baxter Healthcare Corporation
Plasma-Lyte A is a injection, solution containing sodium chloride, sodium gluconate, sodium acetate, potassium chloride and magnesium chloride at 30 mg/100mL, taken intravenous. Manufactured by Baxter Healthcare Corporation.
Key Facts
- Brand Name
- Plasma-Lyte A
- Generic Name
- Sodium Chloride, Sodium Gluconate, Sodium Acetate, Potassium Chloride and Magnesium Chloride
- NDC Code (Product)
0338-0221- Manufacturer
- Baxter Healthcare Corporation
- Strength
- 30 mg/100mL
- Dosage Form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Marketing Status
- Application #
- NDA017378
- Marketing Start
- 02/02/1979
Recall History
No Recall HistoryFrequently Asked Questions
What is Plasma-Lyte A used for?
Plasma-Lyte A contains Sodium Chloride, Sodium Gluconate, Sodium Acetate, Potassium Chloride and Magnesium Chloride. It is a injection, solution taken intravenous. Consult your doctor for specific uses.
Is Plasma-Lyte A a controlled substance?
Plasma-Lyte A is not classified as a controlled substance by the DEA.
What is the generic name for Plasma-Lyte A?
The generic name for Plasma-Lyte A is Sodium Chloride, Sodium Gluconate, Sodium Acetate, Potassium Chloride and Magnesium Chloride. There are 2 other brand versions of Sodium Chloride, Sodium Gluconate, Sodium Acetate, Potassium Chloride and Magnesium Chloride.
What is the NDC code for Plasma-Lyte A 30 mg/100mL?
The NDC (National Drug Code) for Plasma-Lyte A 30 mg/100mL is 0338-0221, listed by Baxter Healthcare Corporation.