United States · FDA National Drug Code directory
Potassium Chloride Extended-Release
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
- 24979-232_57726ba4-17f1-4613-8ab9-e64f3f155e8e
- Product NDC
- 24979-232
- Form
- TABLET, EXTENDED RELEASE
- Composition / generic term
- Potassium Chloride
- Labeler
- Upsher-Smith Laboratories, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230410
- Source listing expiry
- 20271231
Source-listed ingredients
- POTASSIUM CHLORIDE — 1500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (24979-232-01) · 24979-232-01
- 500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (24979-232-02) · 24979-232-02
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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