FDA.reportPublic FDA data

NDC 57926-465 - 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
57926-465
Package NDCs from labels
57926-465-01
Manufacturer
Merck Sharp & Dohme Corp.
Effective date
2024-11-15
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
SALIX ® (furosemide injection)Merck Sharp & Dohme Corp.2024-11-15PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
57926-465-01Salix1 in 1 CARTONINJECTION15
57926-465-01Salix50 mL in 1 VIAL, MULTI-DOSEINJECTION505

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
57926-465SALIX (FUROSEMIDE) INJECTION [MERCK SHARP & DOHME CORP.]52 package rows20241120_c3ff7e14-8232-40df-a5c8-60f98f5c1025.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
FurosemideACTIVE INGREDIENT7LXU5N7ZO5SALIX (FUROSEMIDE) INJECTION [MERCK SHARP & DOHME CORP.]2
FurosemideACTIVE MOIETY7LXU5N7ZO5SALIX (FUROSEMIDE) INJECTION [MERCK SHARP & DOHME CORP.]2
DiethanolamineINACTIVE INGREDIENTAZE05TDV2VSALIX (FUROSEMIDE) INJECTION [MERCK SHARP & DOHME CORP.]2
Edetate DisodiumINACTIVE INGREDIENT7FLD91C86KSALIX (FUROSEMIDE) INJECTION [MERCK SHARP & DOHME CORP.]2
Hydrochloric AcidINACTIVE INGREDIENTQTT17582CBSALIX (FUROSEMIDE) INJECTION [MERCK SHARP & DOHME CORP.]2
NitrogenINACTIVE INGREDIENTN762921K75SALIX (FUROSEMIDE) INJECTION [MERCK SHARP & DOHME CORP.]2
Sodium ChlorideINACTIVE INGREDIENT451W47IQ8XSALIX (FUROSEMIDE) INJECTION [MERCK SHARP & DOHME CORP.]2
Sodium HydroxideINACTIVE INGREDIENT55X04QC32ISALIX (FUROSEMIDE) INJECTION [MERCK SHARP & DOHME CORP.]2
Sodium SulfiteINACTIVE INGREDIENTVTK01UQK3GSALIX (FUROSEMIDE) INJECTION [MERCK SHARP & DOHME CORP.]2
WaterINACTIVE INGREDIENT059QF0KO0RSALIX (FUROSEMIDE) INJECTION [MERCK SHARP & DOHME CORP.]2

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 · 148 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
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
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
FurosemideFUROSEMIDEFresenius Kabi USA, LLC3747bbcd-783d-4baa-bb5b-b6827bf390e32024-12-09Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FUROSEMIDEFUROSEMIDEDevatis Inc.c90bcb14-eb8d-4753-b339-3469c664ecd22024-10-31Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDENCS HealthCare of KY, LLC dba Vangard Labs114f4f4f-536a-4658-8fd0-2dd8c029b19a2024-09-17Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEBryant Ranch Prepack25c0aded-ffcd-4145-a48c-76c5fb220f612024-08-23Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEBryant Ranch Prepack0dd28e18-2e15-45eb-9a61-a9de7bd7d64e2024-08-23Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5

Reported adverse events (FAERS/openFDA)#

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