Drugplain

Plasma-Lyte A 30 mg/100mL

Sodium Chloride, Sodium Gluconate, Sodium Acetate, Potassium Chloride and Magnesium Chloride · INJECTION, SOLUTION · Baxter Healthcare Company

No Recall HistoryCurrently in Shortage
Plain English

Plasma-Lyte A is an intravenous solution that replaces fluids and electrolytes in the body. It is commonly used to treat dehydration and maintain proper fluid balance during medical procedures or illness.

Key Facts

Brand Name
Plasma-Lyte A
Generic Name
Sodium Chloride, Sodium Gluconate, Sodium Acetate, Potassium Chloride and Magnesium Chloride
NDC Code (Product)
0338-9591
Manufacturer
Baxter Healthcare Company
Strength
30 mg/100mL
Dosage Form
INJECTION, SOLUTION
Route
INTRAVENOUS
Marketing Status
Marketing Start
11/06/2024

Recall History

No Recall History

Frequently Asked Questions

What is Plasma-Lyte A used for?

Plasma-Lyte A is an intravenous solution that replaces fluids and electrolytes in the body. It is commonly used to treat dehydration and maintain proper fluid balance during medical procedures or illness.

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 0338-9591, listed by Baxter Healthcare Company.

Product NDC

0338-9591

Package NDC

0338-9591-12

Other Plasma-Lyte A Dosages

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)