# Potassium Chloride

NDC: 63629-2620
Generic name: Potassium Chloride
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20181219

FDA application: ANDA210921

## 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:"63629-2620"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63629-2620
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9088ca44-5585-4551-8e2c-168f306520d4
