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
- 63629-2620_d4b99ac9-5f3c-478c-864e-a475f85fd49d
- Product NDC
- 63629-2620
- Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Composition / generic term
- Potassium Chloride
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20181219
- Source listing expiry
- 20271231
Source-listed ingredients
- POTASSIUM CHLORIDE — 600 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-2620-1) · 63629-2620-1
- 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-2620-2) · 63629-2620-2
- 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-2620-3) · 63629-2620-3
- 180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-2620-4) · 63629-2620-4
- 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-2620-5) · 63629-2620-5
- 20 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-2620-6) · 63629-2620-6
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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