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
- 82804-075_61daa681-05a0-4b2f-a6d0-c6fc1044f521
- Product NDC
- 82804-075
- Form
- TABLET, EXTENDED RELEASE
- Composition / generic term
- Potassium Chloride
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20020410
- Source listing expiry
- 20261231
Source-listed ingredients
- POTASSIUM CHLORIDE — 20 meq/1
These values do not establish equivalence or a dose recommendation.
Packages
- 3 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-075-03) · 82804-075-03
- 6 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-075-06) · 82804-075-06
- 10 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-075-10) · 82804-075-10
- 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-075-30) · 82804-075-30
- 60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-075-60) · 82804-075-60
- 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-075-90) · 82804-075-90
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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