FDA.reportPublic FDA data

NDC 0591-0301 - Furosemide

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
0591-0301
Package NDCs from labels
0591-0301-01, 0591-0301-10
Manufacturer
Watson Labs
Effective date
2007-05-28
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Furosemide - Watson LabsWatson Labs2007-05-28HUMAN PRESCRIPTION DRUG LABELING

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0591-0301-01Furosemide100 in 1 BOTTLETABLET1001
0591-0301-10Furosemide1000 in 1 BOTTLETABLET10001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0591-0301FUROSEMIDE (FUROSEMIDE) TABLET [WATSON LABS]12 package rows20070531_A15D7845-5827-481D-BA3F-E4883489A5EF.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
FurosemideACTIVE INGREDIENT7LXU5N7ZO5FUROSEMIDE (FUROSEMIDE) TABLET [WATSON LABS]1
FurosemideACTIVE MOIETY7LXU5N7ZO5FUROSEMIDE (FUROSEMIDE) TABLET [WATSON LABS]1
Corn starchINACTIVE INGREDIENTFUROSEMIDE (FUROSEMIDE) TABLET [WATSON LABS]1
Lactose monohydrateINACTIVE INGREDIENTFUROSEMIDE (FUROSEMIDE) TABLET [WATSON LABS]1
Magnesium stearateINACTIVE INGREDIENT70097M6I30FUROSEMIDE (FUROSEMIDE) TABLET [WATSON LABS]1
Microcrystalline celluloseINACTIVE INGREDIENTFUROSEMIDE (FUROSEMIDE) TABLET [WATSON LABS]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 5 · 96 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
FurosemideFUROSEMIDEAphena Pharma Solutions - Tennessee, LLC3f6529fb-1173-ada3-e063-6294a90a76cb2025-10-13Warnings, Adverse reactionsExact identifier
rxcui: 313988
FurosemideFUROSEMIDEA-S Medication Solutions6194face-c26c-46ed-bde7-1e29bfeabd882025-10-02Warnings, Adverse reactionsExact identifier
rxcui: 313988
LasixFUROSEMIDEValidus Pharmaceuticals LLC2c9b4d8f-0770-482d-a9e6-9c616a440b1a2025-09-30Warnings, Adverse reactionsExact identifier
rxcui: 313988
rxcui: 197732
rxcui: 310429
FurosemideFUROSEMIDEBryant Ranch Prepack53c3f50f-57c6-441b-afea-ec43d7943d1a2025-09-29Warnings, Adverse reactionsExact identifier
rxcui: 310429
FurosemideFUROSEMIDECoupler LLC3eed4bbf-7d0e-e852-e063-6394a90a85c22025-09-16Warnings, Adverse reactionsExact identifier
rxcui: 310429
FurosemideFUROSEMIDEPD-Rx Pharmaceuticals, Inc.48d8f490-e9d1-4c95-ab2f-414d3f4a9df42025-08-18Warnings, Adverse reactionsExact identifier
rxcui: 313988
FurosemideFUROSEMIDEPD-Rx Pharmaceuticals, Inc.c24489c3-65e0-44e3-a50a-8bb0672e88212025-08-15Warnings, Adverse reactionsExact identifier
rxcui: 310429
FurosemideFUROSEMIDEPD-Rx Pharmaceuticals, Inc.52e75604-5766-40e8-a13a-8c449e06ebda2025-08-15Warnings, Adverse reactionsExact identifier
rxcui: 313988
FurosemideFUROSEMIDEPD-Rx Pharmaceuticals, Inc.12137a90-fb35-45d7-8984-0b04793d3e342025-08-15Warnings, Adverse reactionsExact identifier
rxcui: 197732
FUROSEMIDEFUROSEMIDEAurobindo Pharma Limiteda504ee4b-3995-45f2-898c-91116dd81d192025-07-19Warnings, Adverse reactionsExact identifier
rxcui: 313988
rxcui: 197732
rxcui: 310429
FurosemideFUROSEMIDEPD-Rx Pharmaceuticals, Inc.3ba730ab-90d4-478a-80b3-1ea3edb03e4d2025-07-15Warnings, Adverse reactionsExact identifier
rxcui: 310429
FurosemideFUROSEMIDEProficient Rx LP600ca175-be2b-4c43-b119-133ae21a56012025-07-01Warnings, Adverse reactionsExact identifier
rxcui: 313988
FurosemideFUROSEMIDESolco Healthcare LLC6a0fb397-63ae-4fce-bddf-16a91b1b7a2f2025-06-18Warnings, Adverse reactionsExact identifier
rxcui: 313988
rxcui: 197732
rxcui: 310429
UDSxMP Medicated SystemFUROSEMIDE, BENZALKONIUM CHLORIDEWellbeing Medical Supply06b901dc-0f1d-424f-8c4b-a29113cbab252025-06-12Warnings, Adverse reactionsExact identifier
rxcui: 310429
UDSx Medicated SystemFUROSEMIDE, BENZALKONIUM CHLORIDEWellbeing Medical Supply8f1df75b-101a-45da-924a-2767c34a4efe2025-06-12Warnings, Adverse reactionsExact identifier
rxcui: 310429
FurosemideFUROSEMIDEPrefferred Pharmaceuticals Inc.ede9846b-b4c5-4be2-9188-fd65e66cd8932025-04-30Warnings, Adverse reactionsExact identifier
rxcui: 310429
FurosemideFUROSEMIDECoupler LLC33ec71e2-8fbd-0703-e063-6294a90a62e12025-04-29Warnings, Adverse reactionsExact identifier
rxcui: 197732
FurosemideFUROSEMIDEChartwell RX, LLC8ebd2f10-acfc-48a4-a5db-f20377bda9ce2025-03-26Warnings, Adverse reactionsExact identifier
rxcui: 313988
rxcui: 310429
FurosemideFUROSEMIDERising Pharma Holdings, Inc.6101b9b4-f3ef-438e-a857-b4ea55ffc6792025-02-21Warnings, Adverse reactionsExact identifier
rxcui: 313988
rxcui: 197732
rxcui: 310429
FurosemideFUROSEMIDEIpca Laboratories Limited0acd293b-ecab-4879-a8e7-cd1b76148f2a2025-01-20Warnings, Adverse reactionsExact identifier
rxcui: 313988
rxcui: 197732
rxcui: 310429

Reported adverse events (FAERS/openFDA)#

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