# POTASSIUM CHLORIDE

NDC: 71656-022
Generic name: POTASSIUM CHLORIDE
Labeler / Manufacturer: Saptalis Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20231005

FDA application: ANDA211648

## Active ingredients

- POTASSIUM CHLORIDE: 3 g/15mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71656-022"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71656-022
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=483f338e-a164-4c1f-a34e-fef3312cb7ec