# KLOR-CON

NDC: 0245-0835
Generic name: potassium chloride
Labeler / Manufacturer: Upsher-Smith Laboratories, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20250815

FDA application: ANDA218979

## 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:"0245-0835"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0245-0835
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4340c3f2-ecf8-44cd-9b69-217f543e24e2