# Potassium Chloride

NDC: 43386-194
Generic name: Potassium Chloride
Labeler / Manufacturer: Lupin Pharmaceuticals,Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: FOR SOLUTION
Routes: ORAL
Marketing started: 20181121

FDA application: ANDA210241

## Active ingredients

- POTASSIUM CHLORIDE: 1.5 g/1.54g

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"43386-194"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43386-194
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1bbacdbb-91fa-4897-a00c-1b293de27b83