# Potassium Chloride Extended-release

NDC: 17856-1135
Generic name: Potassium Chloride Extended-release
Labeler / Manufacturer: Atlantic Biologicals Corp.
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

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"17856-1135"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=17856-1135
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4d7ad5c6-2c18-dc29-e063-6394a90a621e