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
0615-8442_9738e0ef-5d1c-4a9d-8d51-4c5375d0bda8
Product NDC
0615-8442
Form
CAPSULE, EXTENDED RELEASE
Composition / generic term
Potassium Chloride
Labeler
NCS HealthCare of KY, LLC dba Vangard Labs
Marketing category
ANDA
Marketing start / end (source format)
20210301
Source listing expiry
20261231

Source-listed ingredients

  • POTASSIUM CHLORIDE — 750 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 15 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (0615-8442-05) · 0615-8442-05
  • 30 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (0615-8442-39) · 0615-8442-39

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.

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Potassium Chloride — United States | Molindra Medicines