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 2 of 8 · 159 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
FUROSEMIDEFUROSEMIDEHospira, Inc.aaced7a8-c3d7-4d66-8c07-aa407b8b3f352026-05-13Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDECardinal Health 107, LLC8e0bac29-5a8b-4d4e-93b3-2e21eb3b06502026-05-06Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEPreferred Pharmaceuticals, Inc.a23fc1e0-2d16-43a8-a34e-f6505dcd63162026-04-29Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEPreferred Pharmaceuticals Inc.cad102d7-0197-4cff-bb80-9f0b5bcb599b2026-04-29Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEREMEDYREPACK INC.7181e528-c862-4dd7-8446-9011e4c7312a2026-04-23Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
Caldesene BabySTARCH, CORN AND ZINC OXIDEInsight Pharmaceuticals LLC9f12dee2-7afa-45e9-a729-0fd42bb777152026-04-22WarningsExact identifier
unii: O8232NY3SJ
Caldesene Medicated ProtectingCORNSTARCH AND ZINC OXIDEInsight Pharmaceuticals LLCffc92a0f-a7cf-4a46-b2f1-089df2bbb96b2026-04-22WarningsExact identifier
unii: O8232NY3SJ
FurosemideFUROSEMIDERedpharm Drug37457273-38a1-f938-e063-6294a90a50ab2026-04-15Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.1b9117d5-0dd9-4577-a1fd-bb0aaf7e68ec2026-03-18Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDECoupler LLC4cc2c2d1-2fa4-f6b6-e063-6294a90a290e2026-03-11Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEDirect_Rxe9be5c3b-4b18-7ad2-e053-2995a90a4a8b2026-03-09Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEMarlex Pharmaceuticals, Inc.4bd1b15e-354e-051f-e063-6294a90a3f3b2026-03-01Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDENuCare Pharmaceuticals,Inc.bd45c963-a413-e9a1-e053-2a95a90a14382026-02-19Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEPreferred Pharmaceuticals Inc.adda78ee-0cf5-4613-a748-5d6571afe3542026-01-19Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
Lotrimin Daily Sweat and Odor ControlTOPICAL STARCHBayer HealthCare LLC.9ec5c80d-b550-496f-e053-2a95a90a54892026-01-16WarningsExact identifier
unii: O8232NY3SJ
FUROSEMIDEFUROSEMIDECardinal Health 107, LLC2590ebb6-ce2a-4e23-9244-e54e3010d4882026-01-15Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEAvKAREd4c532be-1f3f-60d3-e053-2995a90a98be2026-01-14Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEMeitheal Pharmaceuticals Inc.a2e3c748-28ce-4c50-a182-7219129198402026-01-14Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEA-S Medication Solutions8f56d6f6-a5ea-4171-9e24-d2fdb11a65f82026-01-13Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEMicro Labs Limited2f547f7c-0322-465c-9764-43f955d98ab22026-01-11Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5

Reported adverse events (FAERS/openFDA)#

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