# Potassium Chloride

NDC: 70436-002
Generic name: Potassium Chloride
Labeler / Manufacturer: Slate Run Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20181115

FDA application: ANDA209314

## Active ingredients

- POTASSIUM CHLORIDE: 750 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70436-002"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70436-002
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0cc57ece-f15a-4160-a5ea-8d6fa9f9e754