# Potassium Chloride

NDC: 64950-321
Generic name: Potassium Chloride
Labeler / Manufacturer: Genus Lifesciences Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: POWDER, FOR SOLUTION
Routes: ORAL
Marketing started: 20150907

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:"64950-321"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=64950-321
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=23d818e7-c076-40de-8dc1-0b51ba4be96a