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
- 68462-357_b0251572-aa7f-434a-a7ff-33ccbc37dfaf
- Product NDC
- 68462-357
- Form
- CAPSULE, EXTENDED RELEASE
- Composition / generic term
- Potassium Chloride
- Labeler
- Glenmark Pharmaceuticals Inc., USA
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20160120
- 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 (68462-357-01) · 68462-357-01
- 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68462-357-05) · 68462-357-05
- 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68462-357-90) · 68462-357-90
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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