# Potassium Chloride Extended-release

NDC: 70010-135
Generic name: Potassium Chloride Extended-release
Labeler / Manufacturer: Granules Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20210130

FDA application: ANDA214452

## Active ingredients

- POTASSIUM CHLORIDE: 1500 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70010-135"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70010-135
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b3d4d5b5-2898-ae3d-e053-2a95a90a6d04