# POTASSIUM CHLORIDE

NDC: 0409-6635
Generic name: POTASSIUM CHLORIDE
Labeler / Manufacturer: Hospira, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION, CONCENTRATE
Routes: INTRAVENOUS
Marketing started: 20050919

FDA application: ANDA080205

## Active ingredients

- POTASSIUM CHLORIDE: 149 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0409-6635"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0409-6635
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=559a0a8c-a8fe-40a5-b196-21f9308780ab