# Potassium Chloride

NDC: 0603-1554
Generic name: Potassium Chloride
Labeler / Manufacturer: Endo USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: POWDER, FOR SOLUTION
Routes: ORAL
Marketing started: 20150918

FDA application: NDA208019

## 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:"0603-1554"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0603-1554
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a64d7151-09a6-474c-83fc-36c7cf582d32