# Potassium Citrate

NDC: 65841-538
Generic name: Potassium Citrate
Labeler / Manufacturer: Zydus Lifesciences Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20140812

FDA application: ANDA203546

## 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:"65841-538"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65841-538
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=39f46084-fc4b-4bfc-91cb-9be7e647655a