# Potassium Chloride

NDC: 69543-451
Generic name: Potassium Chloride
Labeler / Manufacturer: Virtus Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: POWDER, FOR SOLUTION
Routes: ORAL
Marketing started: 20210101
Marketing ended: 20260831
FDA application: ANDA210200

## Active ingredients

- POTASSIUM CHLORIDE: 1.5 g/1.77g

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"69543-451"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69543-451
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b43b84ea-babd-477b-b69b-811657bc1503