# Potassium Chloride

NDC: 63739-972
Generic name: potassium chloride
Labeler / Manufacturer: Mckesson Corporation DBA SKY Packaginng
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 19981120
Marketing ended: 20260831
FDA application: ANDA074726

## Active ingredients

- POTASSIUM CHLORIDE: 750 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63739-972"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63739-972
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5cccc39f-6a6d-415e-a55f-f4ee57f72a0a