NDC 65862-987-06 - Potassium Chloride
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 65862-987
- Requested NDC
- 65862-987-06
- Package NDCs from labels
- 65862-987-01, 65862-987-99, 65862-987-04, 65862-987-80, 65862-987-06, 65862-987-12
- Manufacturer
- Preferred Pharmaceuticals Inc.
- Effective date
- 2026-08-17
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Potassium Chloride - Preferred Pharmaceuticals Inc. | Preferred Pharmaceuticals Inc. | 2026-08-17 | HUMAN PRESCRIPTION DRUG LABEL |
| Potassium Chloride - REMEDYREPACK INC. | REMEDYREPACK INC. | 2026-07-31 | HUMAN PRESCRIPTION DRUG LABEL |
| Potassium Chloride - Northwind Health Company, LLC | Northwind Health Company, LLC | 2026-01-01 | HUMAN PRESCRIPTION DRUG LABEL |
| Potassium Chloride - Major Pharmaceuticals | Major Pharmaceuticals | 2025-09-22 | HUMAN PRESCRIPTION DRUG LABEL |
| Potassium Chloride - Aphena Pharma Solutions - Tennessee, LLC | Aphena Pharma Solutions - Tennessee, LLC | 2025-09-04 | HUMAN PRESCRIPTION DRUG LABEL |
| Potassium Chloride - American Health Packaging | American Health Packaging | 2024-01-22 | HUMAN PRESCRIPTION DRUG LABEL |
| Potassium Chloride - A-S Medication Solutions | A-S Medication Solutions | 2023-09-18 | Human Prescription Drug Label |
| Potassium Chloride - Aurobindo Pharma Limited | APL HEALTHCARE LIMITED | Aurobindo Pharma Limited | APL HEALTHCARE LIMITED | 2021-04-29 | Human Prescription Drug Label |
| Potassium Chloride - Denton Pharma, Inc. DBA Northwind Pharmaceuticals | Denton Pharma, Inc. DBA Northwind Pharmaceuticals | 2020-02-17 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 65862-987-01 | Potassium Chloride | 100 in 1 BOTTLE | TABLET, FILM COATED, EXTENDED RE | 100 | 4 | |
| 65862-987-04 | Potassium Chloride | 4 in 1 BLISTER PACK | TABLET, FILM COATED, EXTENDED RE | 4 | 4 | |
| 65862-987-06 | Potassium Chloride | 6 in 1 BLISTER PACK | TABLET, FILM COATED, EXTENDED RE | 6 | 4 | |
| 65862-987-12 | Potassium Chloride | 120 in 1 CARTON | TABLET, FILM COATED, EXTENDED RE | 120 | 4 | |
| 65862-987-80 | Potassium Chloride | 80 in 1 CARTON | TABLET, FILM COATED, EXTENDED RE | 80 | 4 | |
| 65862-987-99 | Potassium Chloride | 1000 in 1 BOTTLE | TABLET, FILM COATED, EXTENDED RE | 1000 | 4 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 65862-987-01 | EA - Each | 65862-987 | 5b0a20e1-887f-40f2-a4b6-b83ed5141aed | 1 | 2019-03-12 |
| 65862-987-99 | EA - Each | 65862-987 | 2152d0a9-3701-4e34-9a07-e946557e0cc0 | 1 | 2019-03-12 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.