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
- 0832-5325_39990061-98d4-6669-e063-6394a90ae067
- Product NDC
- 0832-5325
- Form
- TABLET, EXTENDED RELEASE
- Composition / generic term
- potassium chloride
- Labeler
- Upsher-SmithLaboratories, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 19981120
- Source listing expiry
- 20261231
Source-listed ingredients
- POTASSIUM CHLORIDE — 1500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (0832-5325-10) · 0832-5325-10
- 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0832-5325-11) · 0832-5325-11
- 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (0832-5325-15) · 0832-5325-15
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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