# Potassium Chloride

NDC: 62037-560
Generic name: Potassium Chloride
Labeler / Manufacturer: Actavis Pharma, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20080825
Marketing ended: 20261031
FDA application: ANDA077419

## 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:"62037-560"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=62037-560
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ed5baaf6-270b-4dd3-b100-36030c0098fc