United States · FDA National Drug Code directory
Potassium Chloride
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
- 59651-430_d1038d80-ef7d-456a-9f47-0c5df1ca8811
- Product NDC
- 59651-430
- Form
- TABLET, EXTENDED RELEASE
- Composition / generic term
- Potassium Chloride
- Labeler
- Aurobindo Pharma Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210331
- Source listing expiry
- 20261231
Source-listed ingredients
- POTASSIUM CHLORIDE — 1125 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (59651-430-01) · 59651-430-01
- 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (59651-430-99) · 59651-430-99
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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