# Potassium Citrate

NDC: 72162-1759
Generic name: Potassium Citrate
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20200316

FDA application: ANDA212779

## Active ingredients

- POTASSIUM CITRATE: 15 meq/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72162-1759"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72162-1759
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6271d84e-d991-4bb8-ac9f-6d5cc879b631