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
50090-7379_9f4620c9-bb6f-46c3-abec-5bd77ea4e41a
Product NDC
50090-7379
Form
TABLET, FILM COATED, EXTENDED RELEASE
Composition / generic term
Potassium Chloride
Labeler
A-S Medication Solutions
Marketing category
ANDA
Marketing start / end (source format)
20230807
Source listing expiry
20271231

Source-listed ingredients

  • POTASSIUM CHLORIDE — 750 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7379-0) · 50090-7379-0

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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