# Potassium chloride extended release

NDC: 55154-6709
Generic name: Potassium chloride
Labeler / Manufacturer: Cardinal Health 107, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20151211
Marketing ended: 20260531
FDA application: ANDA205993

## Active ingredients

- POTASSIUM CHLORIDE: 10 meq/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"55154-6709"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55154-6709
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=446ad1bd-cf5c-41a7-945f-a6575cab16bf