# Potassium Chloride

NDC: 70010-147
Generic name: Potassium Chloride
Labeler / Manufacturer: Granules Pharmaceuticals Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20210301

FDA application: ANDA214686

## Active ingredients

- POTASSIUM CHLORIDE: 600 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70010-147"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70010-147
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c1f4832d-4d5c-8c49-e053-2a95a90ac9fe