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
- 71656-021_4872fd4b-ae1d-9c4c-e063-6294a90a7fc6
- Product NDC
- 71656-021
- Form
- SOLUTION
- Composition / generic term
- POTASSIUM CHLORIDE ORAL
- Labeler
- Saptalis Pharmaceuticals, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20231005
- Source listing expiry
- 20271231
Source-listed ingredients
- POTASSIUM CHLORIDE — 1.5 g/15mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 TRAY in 1 CASE (71656-021-01) / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE (71656-021-15) · 71656-021-01
- 10 TRAY in 1 CASE (71656-021-02) / 10 CUP, UNIT-DOSE in 1 TRAY / 30 mL in 1 CUP, UNIT-DOSE (71656-021-30) · 71656-021-02
- 473 mL in 1 BOTTLE (71656-021-16) · 71656-021-16
- 5 TRAY in 1 CASE (71656-021-50) / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE (71656-021-15) · 71656-021-50
- 5 TRAY in 1 CASE (71656-021-51) / 10 CUP, UNIT-DOSE in 1 TRAY / 30 mL in 1 CUP, UNIT-DOSE (71656-021-30) · 71656-021-51
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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