NDC 0338-0221 – Plasma-Lyte A

Sodium Chloride 526 mg/100mL; Sodium Gluconate 502 mg/100mL; Sodium Acetate 368 mg/100mL; Potassium Chloride 37 mg/100mL; Magnesium Chloride 30 mg/100mL · Injection, Solution · Intravenous

Human Prescription Drug

Product NDC0338-0221

Product details

Brand name
Plasma-Lyte A
Generic name
Sodium Chloride, Sodium Gluconate, Sodium Acetate, Potassium Chloride and Magnesium Chloride
Labeler
Baxter Healthcare Corporation
Dosage form
Injection, Solution
Route
Intravenous
Marketing category
NDA · NDA017378
Marketed since
February 2, 1979
Listing expires
December 31, 2027
Pharmacologic class
Calculi Dissolution Agent; Osmotic Laxative; Osmotic Laxative; Osmotic Laxative; Potassium Salt

Active ingredients

Uses, dosage, side effects and warnings for Plasma-Lyte A →

Package NDC codes (2)

Package NDCDescriptionSince
0338-0221-03500 mL in 1 BAG (0338-0221-03)Feb 2, 1979
0338-0221-041000 mL in 1 BAG (0338-0221-04)Feb 2, 1979