# Potassium Chloride

NDC: 0904-7292
Generic name: Potassium Chloride
Labeler / Manufacturer: Major Pharmaceuticals
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20230501
Marketing ended: 20260630
FDA application: ANDA212861

## Active ingredients

- POTASSIUM CHLORIDE: 750 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0904-7292"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0904-7292
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7c2274f2-5a7f-4a4a-8b7b-44f6ef9a84a4