# Potassium Chloride

NDC: 62037-710
Generic name: Potassium Chloride
Labeler / Manufacturer: Actavis Pharma, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20020410
Marketing ended: 20260630
FDA application: ANDA075604

## 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:"62037-710"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=62037-710
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=db002ae3-f54c-40a4-9cb4-e5681bf426e3