# Plasma-Lyte A

NDC: 0338-0221
Generic name: Sodium Chloride, Sodium Gluconate, Sodium Acetate, Potassium Chloride and Magnesium Chloride
Labeler / Manufacturer: Baxter Healthcare Corporation
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 19790202

FDA application: NDA017378

## Active ingredients

- MAGNESIUM CHLORIDE: 30 mg/100mL
- POTASSIUM CHLORIDE: 37 mg/100mL
- SODIUM ACETATE: 368 mg/100mL
- SODIUM CHLORIDE: 526 mg/100mL
- SODIUM GLUCONATE: 502 mg/100mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0338-0221"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0338-0221
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6ec9e61c-2c26-402f-8604-f446b2e34058