# POTASSIUM CHLORIDE

NDC: 43386-168
Generic name: POTASSIUM CHLORIDE
Labeler / Manufacturer: Lupin Pharmaceuticals,Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20180924

FDA application: ANDA209786

## 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:"43386-168"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43386-168
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=28c49165-d8c9-443a-b000-953b8e1ec55c