# Potassium Chloride

NDC: 63323-667
Generic name: Potassium Chloride, Dextrose Monohydrate
Labeler / Manufacturer: Fresenius Kabi USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20210423

FDA application: ANDA212346

## Active ingredients

- DEXTROSE MONOHYDRATE: 5 g/100mL
- POTASSIUM CHLORIDE: 75 mg/100mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63323-667"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63323-667
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=55d9ae37-4553-47e7-a2e3-86b48b5227cd