# Potassium Chloride for Oral Solution

NDC: 70069-823
Generic name: Potassium Chloride
Labeler / Manufacturer: Somerset Therapeutics, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: FOR SOLUTION
Routes: ORAL
Marketing started: 20250410

FDA application: ANDA213467

## Active ingredients

- POTASSIUM CHLORIDE: 1.5 g/1.58g

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70069-823"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70069-823
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=32809eae-1c3f-96fc-e063-6394a90aeaad