# potassium chloride

NDC: 68462-471
Generic name: potassium chloride
Labeler / Manufacturer: Glenmark Pharmaceuticals Inc., USA
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20160726

FDA application: ANDA203562

## 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:"68462-471"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68462-471
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=63bedd99-0596-49d2-ad04-d1d8ac15cc42