FDA.reportPublic FDA data

NDC 70518-4402-00 - Levothyroxine sodium

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
70518-4402
Requested NDC
70518-4402-00
Package NDCs from labels
70518-4402-0, 70518-4402-00
Manufacturer
REMEDYREPACK INC.
Effective date
2026-09-10
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Levothyroxine sodium - REMEDYREPACK INC.REMEDYREPACK INC.2026-09-10HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70518-4402-0Levothyroxine sodium90 in 1 BOTTLETABLET901

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 9 of 18 · 346 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Levothyroxine SodiumLEVOTHYROXINE SODIUMNorthwind Health Company, LLCdb9821db-3fe3-d1cf-e053-2a95a90a02522026-01-01Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 966253
unii: 9J765S329G
Levothyroxine sodiumLEVOTHYROXINE SODIUMNorthwind Health Company, LLCda570872-94a1-4852-e053-2995a90aacb62026-01-01Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA212399
rxcui: 892246
unii: 9J765S329G
Levothyroxine sodiumLEVOTHYROXINE SODIUMNorthwind Health Company, LLCda827567-810b-624d-e053-2a95a90a9bde2026-01-01Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA212399
rxcui: 966225
unii: 9J765S329G
Levothyroxine SodiumLEVOTHYROXINE SODIUMNorthwind Health Company, LLCf86fab39-bbd9-a51c-e053-6294a90accd02026-01-01Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 966220
unii: 9J765S329G
Levothyroxine SodiumLEVOTHYROXINE SODIUMNorthwind Health Company, LLCd9dff641-ced3-bae3-e053-2a95a90a2e292026-01-01Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 966221
unii: 9J765S329G
Levothyroxine SodiumLEVOTHYROXINE SODIUMCoupler LLC472ec9e7-c1db-bf8c-e063-6394a90a2c072025-12-30Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 966222
unii: 9J765S329G
Dem ZeroPHOSPHATIDYLSERINE, MAGNESIUM OXIDENPG Bio Pharmaceuticals Co.,Ltd.411f1a0f-ed02-cc78-e063-6394a90a0aec2025-12-18WarningsExact identifier
unii: 3A3U0GI71G
Alzh LPHOSPHATIDYLSERINE, MAGNESIUM OXIDENPG Bio Pharmaceuticals Co.,Ltd.41056de0-aaa2-01bb-e063-6394a90af7b82025-12-18WarningsExact identifier
unii: 3A3U0GI71G
Levothyroxine SodiumLEVOTHYROXINE SODIUMA-S Medication Solutionse3667ab1-2bd9-4e0d-8a97-f907593e79542025-12-16Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 966248
unii: 9J765S329G
Levothyroxine SodiumLEVOTHYROXINE SODIUMA-S Medication Solutionseb120047-a43b-40a4-9f55-067b1b51edda2025-12-16Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 966248
unii: 9J765S329G
LEVOTHYROXINE SODIUMLEVOTHYROXINE SODIUMA-S Medication Solutions2adb05ef-b3fa-4ac2-b219-99442746392b2025-12-04Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 966270
unii: 9J765S329G
LEVOTHYROXINE SODIUMLEVOTHYROXINE SODIUMA-S Medication Solutionsd5b005e8-a88d-450b-bbc3-393d885260f52025-12-04Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 966270
unii: 9J765S329G
Levothyroxine sodiumLEVOTHYROXINE SODIUMA-S Medication Solutionsc29a417b-95b0-4c9b-85e6-ec884049edb12025-12-02Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA212399
rxcui: 966222
unii: 9J765S329G
Levothyroxine sodiumLEVOTHYROXINE SODIUMA-S Medication Solutions3453af75-8c2e-421f-9a08-24751936df412025-12-01Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA212399
rxcui: 966225
unii: 9J765S329G
Levothyroxine sodiumLEVOTHYROXINE SODIUMA-S Medication Solutions1af49c9f-93da-4838-899b-9445083a154b2025-12-01Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA212399
rxcui: 966225
unii: 9J765S329G
Prenate ChewableCALCIUM CARBONATE, CHOLECALCIFEROL, MAGNESIUM OXIDE, BORON, FOLIC ACID, LEVOMEFOLATE GLUCOSAMINE, PYRIDOXINE HYDROCHLORIDE, CYANOCOBALAMIN, BIOTIN AND BLUEBERRYAvion Pharmaceuticals, LLC917f02ce-51b9-4819-81e0-522842f6732a2025-11-25Adverse reactionsExact identifier
unii: 3A3U0GI71G
Levothyroxine SodiumLEVOTHYROXINE SODIUMA-S Medication Solutionsfea284d8-0514-498b-a37c-405730b5f6a22025-11-18Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 966270
unii: 9J765S329G
Magnesium OxideMAGNESIUM OXIDEMarlex Pharmaceuticals Inc0bb322a5-fb92-14de-e063-6294a90a4c1b2025-11-14WarningsExact identifier
unii: 3A3U0GI71G
magnesium oxideMAGNESIUM OXIDEMarlex Pharmaceuticals Inc.dc57893c-068a-37d8-e053-2a95a90aa0542025-11-14WarningsExact identifier
unii: 3A3U0GI71G
Levothyroxine SodiumLEVOTHYROXINE SODIUMCoupler LLC4302e36f-0b5b-f645-e063-6394a90a010f2025-11-07Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 966224
unii: 9J765S329G

Reported adverse events (FAERS/openFDA)#

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