# POTASSIUM CHLORIDE

NDC: 60687-628
Generic name: POTASSIUM CHLORIDE
Labeler / Manufacturer: American Health Packaging
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20220228
Marketing ended: 20261231
FDA application: ANDA211648

## Active ingredients

- POTASSIUM CHLORIDE: 1.5 g/15mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"60687-628"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60687-628
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7956883f-0d31-4081-bbea-d9ea320a193b