FDA.reportPublic FDA data

NDC 57926-464 - Salix

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
57926-464
Package NDCs from labels
57926-464-31
Manufacturer
Merck Sharp & Dohme Corp.
Effective date
2025-10-30
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Salix ® (furosemide tablets)Merck Sharp & Dohme Corp.2025-10-30PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
57926-464-31Salix500 in 1 BOTTLETABLET5007

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
57926-464SALIX (FUROSEMIDE) TABLET [MERCK SHARP & DOHME CORP.]61 package rows20250503_9ad8eb8a-7c65-4746-9c03-1d6136b5892c.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
FurosemideACTIVE INGREDIENT7LXU5N7ZO5SALIX (FUROSEMIDE) TABLET [SCHERING CORPORATION]1
FurosemideACTIVE MOIETY7LXU5N7ZO5SALIX (FUROSEMIDE) TABLET [SCHERING CORPORATION]1
Cellulose, MicrocrystallineINACTIVE INGREDIENTOP1R32D61USALIX (FUROSEMIDE) TABLET [SCHERING CORPORATION]1
FD&C Yellow No. 5INACTIVE INGREDIENTI753WB2F1MSALIX (FUROSEMIDE) TABLET [SCHERING CORPORATION]1
Lactose MonohydrateINACTIVE INGREDIENTEWQ57Q8I5XSALIX (FUROSEMIDE) TABLET [SCHERING CORPORATION]1
Magnesium StearateINACTIVE INGREDIENT70097M6I30SALIX (FUROSEMIDE) TABLET [SCHERING CORPORATION]1
Starch, CornINACTIVE INGREDIENTO8232NY3SJSALIX (FUROSEMIDE) TABLET [SCHERING CORPORATION]1

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 5 of 8 · 159 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
FUROSEMIDEFUROSEMIDEAurobindo Pharma Limiteda504ee4b-3995-45f2-898c-91116dd81d192025-07-19Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEPD-Rx Pharmaceuticals, Inc.3ba730ab-90d4-478a-80b3-1ea3edb03e4d2025-07-15Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDENorthStar Rx LLCfc3194a3-7e75-4551-8334-4a5cc22d9f8b2025-07-07Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEProficient Rx LP600ca175-be2b-4c43-b119-133ae21a56012025-07-01Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FUROSEMIDEFUROSEMIDEBaxter Healthcare Corporationc71371a7-75c5-45b8-b762-8d782d4c71bc2025-06-30Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDESagent Pharmaceuticalsd76bd85a-8e57-477e-9607-c9435f1e26fb2025-06-26Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDESolco Healthcare LLC6a0fb397-63ae-4fce-bddf-16a91b1b7a2f2025-06-18Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEMaiva Pharma Private Limitede5880bf4-5037-4813-b7cc-656a6832ecb52025-06-13WarningsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEPrefferred Pharmaceuticals Inc.ede9846b-b4c5-4be2-9188-fd65e66cd8932025-04-30Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDECoupler LLC33ec71e2-8fbd-0703-e063-6294a90a62e12025-04-29Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEChartwell RX, LLC8ebd2f10-acfc-48a4-a5db-f20377bda9ce2025-03-26Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEHikma Pharmaceuticals USA Inc.ddfc41a9-37d4-49c1-bbf3-969a98cd649c2025-03-10Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEAvenacy Inc.7d0db0f7-bf4f-4b0b-9359-2a838626e04b2025-02-28Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
YVTYVT MICRODERMABRASION FACIAL SCRUBYVTYVT MICRODERMABRASION FACIAL SCRUBBeijing JUNGE Technology Co., Ltd.2f30fc45-42e2-c766-e063-6394a90a8d682025-02-28WarningsExact identifier
unii: OP1R32D61U
FurosemideFUROSEMIDERising Pharma Holdings, Inc.6101b9b4-f3ef-438e-a857-b4ea55ffc6792025-02-21Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDECamber Pharmaceuticals, Inc.f6221cce-e586-4002-bd14-6ec22eb14e2e2025-01-30Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEIpca Laboratories Limited0acd293b-ecab-4879-a8e7-cd1b76148f2a2025-01-20Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDENuCare Pharmaceuticals,Inc.809d9734-12dd-3b1f-e053-2a91aa0aadee2025-01-02Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDENuCare Pharmaceuticals,Inc.813c8e9b-61bc-27c4-e053-2a91aa0a9f452024-12-26Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEFresenius Kabi USA, LLCc794c95a-654e-48fe-9596-201fc122ff752024-12-09Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5

Reported adverse events (FAERS/openFDA)#

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