# Potassium Chloride

NDC: 0378-4560
Generic name: potassium chloride
Labeler / Manufacturer: Mylan Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20161109
Marketing ended: 20261231
FDA application: ANDA204662

## Active ingredients

- POTASSIUM CHLORIDE: 8 meq/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0378-4560"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0378-4560
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c64ed4c0-1e27-42b3-9625-fb4e0d31e271