FDA.reportPublic FDA data

NDC 50090-5960-01 - Losartan Potassium and Hydrochlorothiazide

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
50090-5960
Requested NDC
50090-5960-01
Package NDCs from labels
50090-5960-0, 50090-5960-2, 50090-5960-1, 50090-5960-01
Manufacturer
A-S Medication Solutions
Effective date
2024-05-06
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Losartan Potassium and Hydrochlorothiazide - A-S Medication SolutionsA-S Medication Solutions2024-05-06HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50090-5960-0Losartan Potassium and Hydrochlorothiazide30 in 1 BOTTLETABLET, FILM COATED307
50090-5960-1Losartan Potassium and Hydrochlorothiazide90 in 1 BOTTLETABLET, FILM COATED907
50090-5960-2Losartan Potassium and Hydrochlorothiazide100 in 1 BOTTLETABLET, FILM COATED1007

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50090-5960LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE (LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE) TABLET, FILM COATED [A-S MEDICATION SOLUTIONS]7Current NDC, Legacy NDC, 3 package rows20240511_1bb08103-04ee-47a6-a9ad-290e169feb51.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50090-5960-0EA - Each50090-5960236055f1-416d-4476-9b0a-73e1e0487b4e12022-07-06
50090-5960-1EA - Each50090-59607d68ca49-dafa-447b-a05c-8d0bc0a3e14112022-07-06
50090-5960-2EA - Each50090-59604e10ae2d-dd32-475b-9ed6-a7938f3dac2512023-04-07

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 4 of 136 · 2,712 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Losartan PotassiumLOSARTAN POTASSIUMZydus Pharmaceuticals USA Inc.3233c707-70b6-4c29-8210-913eeb2a38ed2026-07-20Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 3ST302B24A
Losartan PotassiumLOSARTAN POTASSIUMREMEDYREPACK INC.f7cf8a7d-90f1-46a3-abff-1eb316aa7d722026-07-17Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 3ST302B24A
HYDROCHLOROTHIAZIDEHYDROCHLOROTHIAZIDEBryant Ranch Prepack03b7e52e-0003-47c3-af12-93ef00800b372026-07-16Warnings, Adverse reactionsExact identifier
unii: 0J48LPH2TH
Losartan Potassium and HydrochlorothiazideLOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDELupin Pharmaceuticals, Inc.ee1eaaf6-050b-48af-942b-5e3451edc1642026-07-16Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 979468
rxcui: 979471
rxcui: 979464
unii: 3ST302B24A
unii: 0J48LPH2TH
Losartan PotassiumLOSARTANPreferred Pharmaceuticals Inc.9501dfaa-c8cf-46d6-8bec-936c4fd8fe032026-07-16Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 3ST302B24A
Triamterene and HydrochlorothiazideTRIAMTERENE AND HYDROCHLOROTHIAZIDESandoz Incf824b6ba-bd1c-41a8-8f6f-ad507b48f3e02026-07-16Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 0J48LPH2TH
olmesartan medoxomil-hydrochlorothiazideOLMESARTAN MEDOXOMIL-HYDROCHLOROTHIAZIDEAvKARE569596a2-98f0-116a-e063-6294a90a3fa12026-07-14Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 0J48LPH2TH
Enalapril Maleate and HydrochlorothiazideENALAPRIL MALEATE AND HYDROCHLOROTHIAZIDESun Pharmaceutical Industries, Inc.7cb92cf2-46f2-4379-937c-168d230e43a42026-07-14Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 0J48LPH2TH
Losartan PotassiumLOSARTAN POTASSIUMREMEDYREPACK INC.6f39f7f9-edac-45ca-9ee2-c2ecad0915ab2026-07-10Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 3ST302B24A
Bombee Honey Daily Glow Shield SunscreenHOMOSALATE, OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDEABT ASIA Inc.56112dff-b091-7a56-e063-6294a90a77d32026-07-08WarningsExact identifier
unii: 15FIX9V2JP
HydrochlorothiazideHYDROCHLOROTHIAZIDEPD-Rx Pharmaceuticals, Inc.cb7b7315-0170-492c-803f-60a6e75e55da2026-07-08Warnings, Adverse reactionsExact identifier
unii: 0J48LPH2TH
Triamterene and HydrochlorothiazideTRIAMTERENE AND HYDROCHLOROTHIAZIDEPD-Rx Pharmaceuticals, Inc.f083c321-3170-4982-b5cd-d3fdff7548572026-07-08Warnings, Adverse reactionsExact identifier
unii: 0J48LPH2TH
Stay Ageless Tinted Mineral SunscreenBROAD SPECTRUM SPF30DERMIO DERMATOLOGY LLC562f5b0d-6a10-305d-e063-6394a90a59802026-07-08WarningsExact identifier
unii: 15FIX9V2JP
Stay Ageless Tinted Mineral SunscreenBROAD SPECTRUM SPF30Suzanne's Skin2soul LLC562fbaa6-f93a-5ec4-e063-6294a90a96342026-07-08WarningsExact identifier
unii: 15FIX9V2JP
Aussie Betta Tallow Sunscreen SPF50 SPF50TITANIUM DIOXIDE AND ZINC OXIDE SUNSCREENAUSSIE BETTA HEALTHY CARE PTY LTD56007d82-ff5b-6c26-e063-6294a90a09b62026-07-07WarningsExact identifier
unii: 15FIX9V2JP
Artificial TearsARTIFICIAL TEARSAvPAKf18bebf2-1936-658f-e053-2a95a90a50122026-07-07WarningsExact identifier
unii: 3NXW29V3WO
Irbesartan and HydrochlorothiazideIRBESARTAN AND HYDROCHLOROTHIAZIDEREMEDYREPACK INC.88aaa2a1-13be-4f56-ace6-66e8990280072026-07-07Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 0J48LPH2TH
Losartan PotassiumLOSARTAN POTASSIUMPD-Rx Pharmaceuticals, Inc.1843ee4b-1afc-4992-993a-4b0e03e785fc2026-07-07Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 3ST302B24A
Losartan PotassiumLOSARTAN POTASSIUMPD-Rx Pharmaceuticals, Inc.9b3ddaa2-a835-736a-e053-2995a90aff082026-07-07Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 3ST302B24A
EELHOE Body Coverage PerfectorTITANIUM DIOXIDEShantou Eelhoe Daily Chemical Technology Co., Ltd.5610c3b7-456b-3bc1-e063-6394a90a3fa82026-07-07WarningsExact identifier
unii: 15FIX9V2JP

Reported adverse events (FAERS/openFDA)#

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