# Potassium Chloride

NDC: 0338-0705
Generic name: POTASSIUM 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: 19891226

FDA application: NDA019904

## Active ingredients

- POTASSIUM CHLORIDE: 14.9 g/1000mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0338-0705"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0338-0705
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=092ddee4-572d-4771-8d95-880cea01097e