# POTASSIUM CHLORIDE

NDC: 70010-072
Generic name: POTASSIUM CHLORIDE
Labeler / Manufacturer: Granules Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20210425

FDA application: ANDA213392

## Active ingredients

- POTASSIUM CHLORIDE: 20 meq/15mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70010-072"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70010-072
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=302b3fa7-ea87-4bf1-aae0-6a2d7459de86