# POTASSIUM CHLORIDE

NDC: 59651-960
Generic name: Potassium Chloride
Labeler / Manufacturer: Aurobindo Pharma Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20251120

FDA application: ANDA216536

## Active ingredients

- POTASSIUM CHLORIDE: 40 meq/15mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"59651-960"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=59651-960
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b17d54ca-5885-48d3-96e9-b29ad14f8d76