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 8 of 8 · 148 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
FurosemideFUROSEMIDELeading Pharma, LLCb5c6fcf4-fd37-4fee-8dac-1a3273d95ffe2022-11-11Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEPrecision Dose Inc.4a746634-379b-4847-a965-7607d2a71bed2022-09-21Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEAphena Pharma Solutions - Tennessee, LLC6f124d7d-a19d-4de6-8ea4-719a42eb520b2022-03-10Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FUROSEMIDEFUROSEMIDEHF Acquisition Co LLC, DBA HealthFirstc5d9b063-e3fe-ec2f-e053-2995a90ab3f22021-06-28Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEProficient Rx LPce84359c-2f76-421a-9b2b-79b1c2be2f202021-01-01Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEGland Pharma Limited644704c0-e6a5-4804-bfa6-795c8f83aa7a2020-07-03Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEAphena Pharma Solutions - Tennessee, LLC1d2733ac-6fa6-44d1-96d4-f1a698045ad22018-04-18Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEAphena Pharma Solutions - Tennessee, LLC6fbf7f3d-7566-44d5-9507-c4460238fc912018-02-09Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5

Reported adverse events (FAERS/openFDA)#

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