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
72162-1786_000215d5-841c-4f90-bfd4-de560e5e042a
Product NDC
72162-1786
Form
TABLET, EXTENDED RELEASE
Composition / generic term
Potassium Chloride
Labeler
Bryant Ranch Prepack
Marketing category
ANDA
Marketing start / end (source format)
20191120
Source listing expiry
20261231

Source-listed ingredients

  • POTASSIUM CHLORIDE — 750 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1786-0) · 72162-1786-0
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1786-1) · 72162-1786-1
  • 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1786-2) · 72162-1786-2
  • 360 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1786-4) · 72162-1786-4
  • 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1786-5) · 72162-1786-5
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1786-7) · 72162-1786-7
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1786-9) · 72162-1786-9

Source and coverage

Open FDA National Drug Code directory

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.

Browse United States records →