# POTASSIUM CHLORIDE EXTENDED RELEASE

NDC: 16571-842
Generic name: potassium chloride
Labeler / Manufacturer: Rising Pharma Holdings, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20250213

FDA application: ANDA217412

## Active ingredients

- POTASSIUM CHLORIDE: 600 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"16571-842"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=16571-842
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=947c11ca-ca0c-42df-8cc5-3db06458ca5b