# Potassium Chloride

NDC: 0603-1543
Generic name: Potassium Chloride
Labeler / Manufacturer: Endo USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20150504
Marketing ended: 20260731
FDA application: NDA206814

## Active ingredients

- POTASSIUM CHLORIDE: 40 meq/15mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0603-1543"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0603-1543
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e5214432-3517-4a90-9412-036752bd1139