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
- 50090-7639_a3f72472-21b1-44b3-9758-e65b4e02c681
- Product NDC
- 50090-7639
- Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Composition / generic term
- Potassium Chloride
- Labeler
- A-S Medication Solutions
- Marketing category
- NDA
- Marketing start / end (source format)
- 19860417
- Source listing expiry
- 20261231
Source-listed ingredients
- POTASSIUM CHLORIDE — 750 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7639-0) · 50090-7639-0
- 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7639-1) · 50090-7639-1
- 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7639-2) · 50090-7639-2
- 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7639-3) · 50090-7639-3
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 →