United States · FDA National Drug Code directory
Potassium Citrate
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 65841-537_042721ed-7f5d-47f1-beff-b54ba88bcd27
- Product NDC
- 65841-537
- Form
- TABLET, EXTENDED RELEASE
- Composition / generic term
- Potassium Citrate
- Labeler
- Zydus Lifesciences Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20140812
- Source listing expiry
- 20261231
Source-listed ingredients
- POTASSIUM CITRATE — 10 meq/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (65841-537-01) · 65841-537-01
- 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (65841-537-05) · 65841-537-05
- 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (65841-537-06) · 65841-537-06
- 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (65841-537-10) · 65841-537-10
- 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (65841-537-16) · 65841-537-16
- 10 BLISTER PACK in 1 CARTON (65841-537-30) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK · 65841-537-30
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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