FDA.reportPublic FDA data

NDC 50090-6982-01 - 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
50090-6982
Requested NDC
50090-6982-01
Package NDCs from labels
50090-6982-1, 50090-6982-0, 50090-6982-01
Manufacturer
A-S Medication Solutions
Effective date
2026-01-14
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Levothyroxine Sodium - A-S Medication SolutionsA-S Medication Solutions2026-01-14HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50090-6982-0Levothyroxine Sodium30 in 1 BOTTLETABLET309
50090-6982-1Levothyroxine Sodium90 in 1 BOTTLETABLET909

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50090-6982LEVOTHYROXINE SODIUM TABLET [A-S MEDICATION SOLUTIONS]7Current NDC, 2 package rows20231229_e2291336-1188-48f4-af52-d12ac892f80f.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50090-6982-0EA - Each50090-6982532ca8c0-7614-4d20-a2b6-8a6b21a30b3612024-02-14
50090-6982-1EA - Each50090-69826f035a2b-177b-4987-a1a4-475d43b62ea012024-02-14

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 8 of 25 · 491 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
LEVOTHYROXINE SODIUMLEVOTHYROXINE SODIUMA-S Medication Solutions1ac29774-2b53-4a3f-97fa-16c2880a08682026-02-06Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 966224
unii: 9J765S329G
Levothyroxine sodiumLEVOTHYROXINE SODIUMA-S Medication Solutionsb717aff6-f754-458d-be87-d12d87c5da002026-02-02Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 966253
unii: 9J765S329G
Levothyroxine sodiumLEVOTHYROXINE SODIUMA-S Medication Solutions62de26a8-d6fc-463f-abe6-4656228c31422026-02-02Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 966253
unii: 9J765S329G
ADRIAN BICARBONATO SODIUM BICARBONATE USP-4 oz, 8 oz and 16 ozSODIUM BICARBONATEEvi Labs4979a339-4ad4-9cdd-e063-6394a90a0acc2026-01-28WarningsExact identifier
unii: 8MDF5V39QO
Levothyroxine SodiumLEVOTHYROXINE SODIUMNorthwind Health Company, LLCffc34bc6-5de5-addb-e053-6294a90a25be2026-01-26Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA209713
rxcui: 892251
unii: 9J765S329G
Levothyroxine SodiumLEVOTHYROXINE SODIUMNuCare Pharmaceuticals, Inc.49136b34-1bc1-ec4e-e063-6394a90ac9dd2026-01-23Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA209713
rxcui: 966220
unii: 9J765S329G
levothyroxine sodiumLEVOTHYROXINE SODIUMA-S Medication Solutionsf2bed4e7-86e9-430e-80d9-7bd7cfcf9bf52026-01-23Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 966224
unii: 9J765S329G
levothyroxine sodiumLEVOTHYROXINE SODIUMA-S Medication Solutions8f7dc71e-4a48-4ba5-945b-f340ff51636e2026-01-23Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 966224
unii: 9J765S329G
Levothyroxine sodiumLEVOTHYROXINE SODIUMA-S Medication Solutions36af0286-e447-4098-b3f2-772debd586672026-01-20Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 966248
unii: 9J765S329G
Levothyroxine sodiumLEVOTHYROXINE SODIUMA-S Medication Solutionse8142948-2bde-4f4b-931e-da43e91f2d592026-01-20Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 966220
unii: 9J765S329G
Levothyroxine sodiumLEVOTHYROXINE SODIUMA-S Medication Solutionsd29bc0fd-5587-4a70-a505-f5aee1f115a62026-01-20Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 966220
unii: 9J765S329G
Levothyroxine sodiumLEVOTHYROXINE SODIUMA-S Medication Solutionsd5b11dac-1acd-4aa2-b837-e3b90d4f69222026-01-20Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 966248
unii: 9J765S329G
Levothyroxine SodiumLEVOTHYROXINE SODIUMNorthwind Health Company, LLCf6c92836-95e1-1402-e053-6394a90a2f5e2026-01-19Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 966270
unii: 9J765S329G
Equate Comfort Flow Sinus washSINUS WASHWALMART INC9e911eef-ca99-9902-e053-2a95a90aab0e2026-01-19WarningsExact identifier
unii: 8MDF5V39QO
Lotrimin Daily Sweat and Odor ControlTOPICAL STARCHBayer HealthCare LLC.9ec5c80d-b550-496f-e053-2a95a90a54892026-01-16WarningsExact identifier
unii: O8232NY3SJ
D-D SUDIUM BICARBONATE U.S.P. BICARBONATO DE SODA PUROSODIUM BICARBONATEEvi Labs485f9eb1-6535-c47c-e063-6394a90ae32c2026-01-14WarningsExact identifier
unii: 8MDF5V39QO
Levothyroxine SodiumLEVOTHYROXINE SODIUMA-S Medication Solutionse2291336-1188-48f4-af52-d12ac892f80f2026-01-14Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA209713
ndc (package): 50090-6982-1
ndc (package): 50090-6982-0
ndc (product): 50090-6982
ndc11 (package): 50090698201
rxcui: 966224
spl id: 48fee4f7-f275-45cf-8d4e-ad207cf91b23
spl set id: e2291336-1188-48f4-af52-d12ac892f80f
unii: 9J765S329G
Levothyroxine SodiumLEVOTHYROXINE SODIUMA-S Medication Solutions98d7ce2b-a248-4ed0-a2ec-d28ba623531e2026-01-14Boxed warning, Warnings, Adverse reactionsExact identifier
application number: ANDA209713
rxcui: 966224
unii: 9J765S329G
levothyroxine sodiumLEVOTHYROXINE SODIUMPreferred Pharmaceuticals, Inc.59a99739-2da5-46a7-8811-1169123bed9b2026-01-13Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 966221
unii: 9J765S329G
levothyroxine sodiumLEVOTHYROXINE SODIUMPreferred Pharmaceuticals, Inc.579b1935-77f5-4381-9cb0-e0130e4834e82026-01-13Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 966248
unii: 9J765S329G

Reported adverse events (FAERS/openFDA)#

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