# Potassium Citrate

NDC: 63629-1966
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: 10 meq/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63629-1966"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63629-1966
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ebf1f1f1-4458-4d34-8432-21698a550e07