NDC 72162-1786-01 - Potassium Chloride Extended-Release
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
- 72162-1786
- Requested NDC
- 72162-1786-01
- Package NDCs from labels
- 72162-1786-1, 72162-1786-2, 72162-1786-4, 72162-1786-5, 72162-1786-7, 72162-1786-9, 72162-1786-0, 72162-1786-01
- Manufacturer
- Bryant Ranch Prepack
- Effective date
- 2024-08-23
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Potassium Chloride Extended-Release - Bryant Ranch Prepack | Bryant Ranch Prepack | 2024-08-23 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 72162-1786-0 | Potassium Chloride Extended-Release | 1000 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 1000 | 106 | |
| 72162-1786-1 | Potassium Chloride Extended-Release | 100 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 100 | 106 | |
| 72162-1786-2 | Potassium Chloride Extended-Release | 180 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 180 | 106 | |
| 72162-1786-4 | Potassium Chloride Extended-Release | 360 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 360 | 106 | |
| 72162-1786-5 | Potassium Chloride Extended-Release | 500 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 500 | 106 | |
| 72162-1786-7 | Potassium Chloride Extended-Release | 100 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 100 | 106 | |
| 72162-1786-9 | Potassium Chloride Extended-Release | 90 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 90 | 106 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 72162-1786 | POTASSIUM CHLORIDE EXTENDED-RELEASE (POTASSIUM CHLORIDE) TABLET, EXTENDED RELEASE [BRYANT RANCH PREPACK] | 106 | Current NDC, 7 package rows | 20240824_863e6980-4a66-48a5-a14f-828a00480c93.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 72162-1786-0 | EA - Each | 72162-1786 | 37d8c011-692c-4550-81c7-0d7f426ade00 | 1 | 2023-10-16 |
| 72162-1786-1 | EA - Each | 72162-1786 | 303977b7-a312-4fed-86a5-f02895c0fdf8 | 1 | 2024-01-04 |
| 72162-1786-2 | EA - Each | 72162-1786 | 90727ca2-caab-47a4-bf31-e677708b0409 | 1 | 2024-01-04 |
| 72162-1786-4 | EA - Each | 72162-1786 | f98fcc5f-bd39-48a7-9d30-c251e05fb9b6 | 1 | 2024-01-04 |
| 72162-1786-5 | EA - Each | 72162-1786 | 0bc6a5dc-1ae4-47c7-9ca4-3c0bd0a9fbb7 | 1 | 2024-01-04 |
| 72162-1786-7 | EA - Each | 72162-1786 | f08f2ed2-f4a0-43b1-beb1-ebc07e93a906 | 1 | 2025-05-14 |
| 72162-1786-9 | EA - Each | 72162-1786 | ecf6c927-f461-4fea-9538-934b5d1c6ba5 | 1 | 2024-01-04 |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| SUTAB | SODIUM SULFATE, MAGNESIUM SULFATE, AND POTASSIUM CHLORIDE | Azurity Pharmaceuticals, Inc. | c020e973-dccf-4862-999e-17db6209a48a | 2026-01-31 | Warnings, Adverse reactions | 660YQ98I10 |
| POKONZA potassium chloride | POTASSIUM CHLORIDE | Carwin Pharmaceutical Associates, LLC | 2d938cbf-27aa-4f9c-a582-5564d3b72465 | 2026-01-22 | Warnings, Adverse reactions | 660YQ98I10 |
| BioMicroneedle PDRN Cream | SILICON DIOXIDE | Guangzhou Shengyanghui Industrial Trading Co., Ltd | 48e2edae-94ea-c42e-e063-6394a90a907b | 2026-01-21 | Warnings | ETJ7Z6XBU4 |
| Inflammation I | ECHINACEA (ANGUSTIFOLIA), NASTURTIUM AQUATICUM, PHYTOLACCA DECANDRA, HYDRASTIS CANADENSIS, APIS MELLIFICA, BELLADONNA, FERRUM PHOSPHORICUM, NITRICUM ACIDUM, OLEANDER, SILICEA | BioActive Nutritional, Inc. | 3cb12181-ae7e-45c7-a1b1-e1952f36f8c3 | 2026-01-21 | Warnings | ETJ7Z6XBU4 |
| DENTI BUONGIORNO PLAQUE CARE LEMON MINT TOOTH | SILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATE, TETRASODIUM PYROPHOSPHATE | ATOSAFE CO., Ltd | 487c5036-0eb0-ada9-e063-6394a90aa02e | 2026-01-16 | Warnings | ETJ7Z6XBU4 |
| DENTI BUONGIORNO PLAQUE CARE LEMON MINT TOOTH | SILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATE, TETRASODIUM PYROPHOSPHATE | DONG IL PHARMS CO.,LTD | 487cd5b9-28f3-392d-e063-6394a90a9ba1 | 2026-01-16 | Warnings | ETJ7Z6XBU4 |
| DENTI BUONGIORNO GUM CARE COOL MINT TOOTH | SILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATE | ATOSAFE CO., Ltd | 487cf27a-d761-6353-e063-6394a90af029 | 2026-01-16 | Warnings | ETJ7Z6XBU4 |
| DENTI BUONGIORNO FRESH BREATH HERB MINT TOOTH | SILICA, SODIUM MONOFLUOROPHOSPHATE | ATOSAFE CO., Ltd | 487d52d1-8853-bc90-e063-6394a90ab91d | 2026-01-16 | Warnings | ETJ7Z6XBU4 |
| DENTI BUONGIORNO GUM CARE COOL MINT TOOTH | SILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATE | DONG IL PHARMS CO.,LTD | 487d689d-ebdd-43c3-e063-6294a90af0e2 | 2026-01-16 | Warnings | ETJ7Z6XBU4 |
| DENTI BUONGIORNO FRESH BREATH HERB MINT TOOTH | SILICA, SODIUM MONOFLUOROPHOSPHATE | DONG IL PHARMS CO.,LTD | 487da363-1d01-8cdc-e063-6294a90ac24d | 2026-01-16 | Warnings | ETJ7Z6XBU4 |
| Berberis Quartz | BERBERIS QUARTZ | Uriel Pharmacy Inc. | 5da48d70-1140-495d-b672-0e55c04196e1 | 2026-01-16 | Warnings | ETJ7Z6XBU4 |
| Potassium Chloride | POTASSIUM CHLORIDE | AvKARE | 755a4a08-04ff-d7d1-a6fc-b8aeff3ae2c6 | 2026-01-15 | Warnings, Adverse reactions | 660YQ98I10 |
| Potassium Chloride | POTASSIUM CHLORIDE | Advagen Pharma Limited | d528c0c1-b81f-4f7a-8518-e6911b23c3eb | 2026-01-13 | Warnings, Adverse reactions | 660YQ98I10 |
| Constipation Relief | ALUMINUM OXIDE, BRYONIA ALBA ROOT, SODIUM CHLORIDE, GRAPHITE, SILICON DIOXIDE | Homeocare Laboratories | 62374240-cd14-44e2-9405-5f8996faf047 | 2026-01-12 | Warnings | ETJ7Z6XBU4 |
| Menopause Relief | BARIUM CARBONATE, ATROPA BELLADONNA, BLACK COHOSH, NITROGLYCERIN, LACHESIS MUTA VENOM, SILICON DIOXIDE | Homeocare Laboratories | 99b182d5-4102-4b25-85d3-f4be077d753f | 2026-01-12 | Warnings | ETJ7Z6XBU4 |
| Amber Amethyst | AMBER AMETHYST | Uriel Pharmacy, Inc | 4837e805-a777-c1fa-e063-6294a90ae9c4 | 2026-01-12 | Warnings | ETJ7Z6XBU4 |
| ECHINACEA | ECHINACEA ANGUSTIFOLIA, HAMAMMELIS VIRGINIANA, CALCAREA PHOSPHORICA, HYDRASTIS CANADANESIS, SENEGA OFFICINALIS, SILICEA, CONIUM, AURUM MURIATICUM NATRONATUM, CALCAREA CARBONICA, FUCUS VESICULOSUS, LACHESIS MUTUS | Marco Pharma International LLC. | 7efadb70-99e4-428b-a8ef-a2797327c6fa | 2026-01-12 | Warnings | ETJ7Z6XBU4 |
| Lung Drainage | ANTIMONIUM ARSENICICUM, BRYONIA (ALBA), CAMPHORA, CARBO VEGETABILIS, CHELIDONIUM MAJUS, CHININUM MURIATICUM, CUPRUM METALLICUM, GELSEMIUM SEMPERVIRENS, HAEMOPHILUS INFLUENZAE B, IPECACUANHA, KALI MURIATICUM, LOBELIA PURPURESCENS, LUNG (SUIS), MYCOPLASMA PNEUMONIAE, MYCOPLASMA PNEUMONIAE DNA, OXYGENIUM, PHOSPHORUS, PNEUMOCOCCINUM, SENEGA OFFICINALIS, STANNUM METALLICUM, VERATRUM VIRIDE | Deseret Biologicals, Inc. | fd109172-46c3-444e-9fa0-124f785c3fb5 | 2026-01-09 | Warnings | 660YQ98I10 |
| Potassium Chloride | POTASSIUM CHLORIDE | AvPAK | f32df7c0-33eb-e6d6-e053-2a95a90a2e8d | 2026-01-09 | Warnings, Adverse reactions | 660YQ98I10 |
| Potassium Chloride | POTASSIUM CHLORIDE | Baxter Healthcare Corporation | 092ddee4-572d-4771-8d95-880cea01097e | 2026-01-09 | Warnings, Adverse reactions | 660YQ98I10 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.