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
- 71335-1747_665b242e-6601-4a0a-af84-338e349e2926
- Product NDC
- 71335-1747
- Form
- TABLET, EXTENDED RELEASE
- Composition / generic term
- potassium chloride
- Labeler
- Bryant Ranch Prepack
- 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
- 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1747-1) · 71335-1747-1
- 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1747-2) · 71335-1747-2
- 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1747-3) · 71335-1747-3
- 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1747-4) · 71335-1747-4
- 15 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1747-5) · 71335-1747-5
- 7 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1747-6) · 71335-1747-6
- 10 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1747-7) · 71335-1747-7
- 3 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1747-8) · 71335-1747-8
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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