# Potassium Chloride

NDC: 0832-5322
Generic name: Potassium Chloride
Labeler / Manufacturer: Upsher-Smith Laboratories, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 19860417

FDA application: NDA019123

## Active ingredients

- POTASSIUM CHLORIDE: 600 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0832-5322"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0832-5322
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=616f0de7-8843-44a1-8fa6-274d889286aa