NDC 70518-4095-4 - 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
70518-4095
Requested NDC
70518-4095-4
Package NDCs from labels
70518-4095-0, 70518-4095-1, 70518-4095-2, 70518-4095-4, 70518-4095-3
Manufacturer
REMEDYREPACK INC.
Effective date
2026-08-27
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Potassium Chloride Extended-Release Tablets USP, 10 mEq and 20 mEq Rx onlyREMEDYREPACK INC.2026-08-27HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70518-4095-0Potassium Chloride Extended-release90 in 1 BOTTLE, PLASTICTABLET, EXTENDED RELEASE905
70518-4095-1Potassium Chloride Extended-release30 in 1 BLISTER PACKTABLET, EXTENDED RELEASE305
70518-4095-2Potassium Chloride Extended-release30 in 1 BLISTER PACKTABLET, EXTENDED RELEASE305
70518-4095-3Potassium Chloride Extended-release50 in 1 BOXTABLET, EXTENDED RELEASE505
70518-4095-4Potassium Chloride Extended-release1 in 1 POUCHTABLET, EXTENDED RELEASE15

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70518-4095POTASSIUM CHLORIDE EXTENDED-RELEASE TABLET, EXTENDED RELEASE [REMEDYREPACK INC.]2Current NDC, 5 package rows20250330_2c407aaf-5d95-49ff-a5db-f1d7b5190334.zip

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.

Matched openFDA labels page 23 of 23 · 447 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Potassium ChloridePOTASSIUM CHLORIDENorthstar Rx LLCdded25a9-3df4-463a-8685-d2bc03ea4edb2018-07-16Warnings, Adverse reactionsExact identifier
unii: 660YQ98I10
Lactated RingersSODIUM CHLORIDE, SOLDIUM LACTATE, POTASSIUM CHLORIDE AND CALCIUM CHLORIDEBaxter Healthcare Company5215ec33-8cfe-4885-ae92-e6a12100bd272018-01-02Warnings, Adverse reactionsExact identifier
unii: 660YQ98I10
Homeoplex FECHINACEA (ANGUSTIFOLIA), PHYTOLACCA DECANDRA, LYMPH NODE (SUIS), CONIUM MACULATUM, FERRUM IODATUM, HEPAR SULPHURIS CALCAREUM, KALI MURIATICUM, LACHESIS MUTUS, SILICEASupplement Clinic, LLC.a1872d34-7298-4016-b7b3-830ac11491262017-11-01WarningsExact identifier
unii: 660YQ98I10
Cardio TonicKALI MURIATICUM, KALI PHOSPHORICUM, PLANTAGO MAJOR, CACTUS GRANDIFLORUS, DIGITALIS PURPUREA, HEART (BOVINE), L-CARNITINE, L-VALINE, THYROIDINUM (SUIS), ABROTANUM (ARTEMISIA ABROTANUM), IODIUM, LECITHIN, SPIGELIA ANTHELMIABioActive Nutritional, Inc.2c252ba6-f147-4c22-b432-cd603a9623ac2017-08-14WarningsExact identifier
unii: 660YQ98I10
TIS-U-SOLSODIUM CHLORIDE, POTASSIUM CHLORIDE, MAGNESIUM SULFATE, SODIUM PHOSPHATE, AND POTASSIUM PHOSPHATEBaxter Healthcare Corporation9da4121f-d62d-4da4-8dfb-0494da16015f2014-02-21Exact identifier
unii: 660YQ98I10
RingersSODIUM CHLORIDE, CALCIUM CHLORIDE, POTASSIUM CHLORIDE,Baxter Healthcare Corporatione1953d54-818d-46a6-8532-518ebae6d84e2012-06-13Exact identifier
unii: 660YQ98I10
Lactated RingersSODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDEBaxter Healthcare Corporationf09f80bf-2f8b-4420-865d-aec2d5e5cd4d2012-06-12Exact identifier
unii: 660YQ98I10

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.