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
- 71335-2045_a54d2cd4-3479-41bb-920f-6d5ba2bf9811
- Product NDC
- 71335-2045
- Form
- TABLET, EXTENDED RELEASE
- Composition / generic term
- Potassium Chloride
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210120
- 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 (71335-2045-1) · 71335-2045-1
- 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2045-2) · 71335-2045-2
- 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2045-3) · 71335-2045-3
- 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2045-4) · 71335-2045-4
- 15 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2045-5) · 71335-2045-5
- 7 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2045-6) · 71335-2045-6
- 10 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2045-7) · 71335-2045-7
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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