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
- 68001-619_42ebb029-df0e-9096-e063-6294a90a9dcc
- Product NDC
- 68001-619
- Form
- CAPSULE, EXTENDED RELEASE
- Composition / generic term
- Potassium Chloride
- Labeler
- BluePoint Laboratories
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240710
- Source listing expiry
- 20261231
Source-listed ingredients
- POTASSIUM CHLORIDE — 750 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68001-619-00) · 68001-619-00
- 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68001-619-03) · 68001-619-03
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 →