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 3 of 8 · 159 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
FurosemideFUROSEMIDEPhlow Corporation08a44bdd-028d-41af-9d4e-70971b0bcc4e2026-01-09Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDENorthwind Health Company, LLC13ba97a7-598a-76a4-e063-6294a90a45c52026-01-02Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FUROSEMIDEFUROSEMIDENorthwind Health Company, LLC1d99e151-75ba-6a75-e063-6294a90a43602026-01-01Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDENorthwind Health Company, LLCf2b920b2-f8b3-1e6e-e053-2a95a90ae1532026-01-01Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDENorthwind Health Company, LLCf3173c0d-2b62-7c7b-e053-2995a90ada052026-01-01Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
Medicated Cornstarch Baby PowderACTIVE CORN STARCHDavion, Inc.e39032d1-c8cd-4a41-af10-126970b8ad382025-12-29WarningsExact identifier
unii: O8232NY3SJ
FurosemideFUROSEMIDERedpharm Drug3745be12-ea1d-f450-e063-6294a90a148c2025-12-24Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEProPharma Distribution38550de1-f099-0cdf-e063-6294a90a9e262025-12-18Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEA-S Medication Solutions54a33042-a163-4f93-96cc-fbd93030e0142025-12-05Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEA-S Medication Solutions6864b3f6-c5ad-4588-ad04-5260258c6d8c2025-12-05Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEQPharma Inc341e29d9-a6f1-4c77-ae44-9b2c423ea6b42025-12-03Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
LASIX ONYUFUROSEMIDESQ Innovation, Inc.cb27654f-c7a1-4796-ab08-60a5fa16f5c02025-11-14Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FUROSEMIDEFUROSEMIDECivica, Inc.7ecaa5af-d186-4380-b105-e7e528f75cc72025-11-12Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEEugia US LLC421aa6d5-623b-4dc2-abd5-bb9e7765bf372025-11-11Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEProPharma Distribution43053bf7-9050-dba8-e063-6294a90a71742025-11-07Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEHikma Pharmaceuticals USA Inc.9e493331-dddd-496e-abf8-61747fb67aba2025-11-03Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDECivica, Inc.6d9caaab-d874-4cf1-b9fe-408452a189982025-10-31Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FUROSEMIDEFUROSEMIDEHenry Schein, Inc.a9853417-0442-4f53-9543-e0749bc3c80d2025-10-31Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEHenry Schein, Inc.d8407b0e-7838-4ab6-b9dd-1f7ecf1e0a172025-10-31Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FUROSEMIDEFUROSEMIDEHenry Schein, Inc.15e4c3a3-7d64-471e-bfdf-6156731e24aa2025-10-31Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5

Reported adverse events (FAERS/openFDA)#

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