# Potassium Chloride

NDC: 0990-7077
Generic name: POTASSIUM CHLORIDE
Labeler / Manufacturer: ICU Medical Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20190401

FDA application: NDA020161

## Active ingredients

- POTASSIUM CHLORIDE: 400 meq/1000mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0990-7077"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0990-7077
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=eb56a807-ea94-4edb-9811-a04b19568468