FDA.reportPublic FDA data

NDC 55154-2348-00 - 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
55154-2348
Requested NDC
55154-2348-00
Package NDCs from labels
55154-2348-0, 55154-2348-00
Manufacturer
Cardinal Health 107, LLC
Effective date
2026-06-18
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Furosemide - Cardinal Health 107, LLCCardinal Health 107, LLC2026-06-18HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55154-2348-0Furosemide1 in 1 BLISTER PACKTABLET13
55154-2348-0Furosemide10 in 1 BAGTABLET103

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55154-2348FUROSEMIDE TABLET [CARDINAL HEALTH 107, LLC]3Current NDC, 2 package rows20250507_2a5bcf50-6d63-463a-915e-a72ea2e5f131.zip

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 1 of 8 · 157 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
FurosemideFUROSEMIDEREMEDYREPACK INC.dba00759-87b4-4ecf-998e-ba03ed3d2f1a2026-08-17Warnings, Adverse reactionsExact identifier
rxcui: 310429
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDERedpharm Drug58d2a38d-75f8-dcb9-e063-6294a90a10d72026-08-12Warnings, Adverse reactionsExact identifier
rxcui: 310429
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEMedical Purchasing Solutions, LLC58cc1e38-6000-1489-e063-6394a90a59782026-08-11Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FUROSCIXFUROSEMIDE INJECTION 80 MG/ 10 MLscPharmaceuticals Inc., a wholly owned subsidiary of MannKind Corporationeac958dd-8d43-e44e-e053-2995a90a4d5e2026-07-31Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEREMEDYREPACK INC.7cdcd001-ab4b-4210-a455-2e17a7bc49722026-07-24Warnings, Adverse reactionsExact identifier
rxcui: 310429
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEREMEDYREPACK INC.3d312ab0-589c-427b-84da-18887244bfc92026-07-15Warnings, Adverse reactionsExact identifier
application number: ANDA076796
rxcui: 310429
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDESt. Mary's Medical Park Pharmacyfebeaf8c-0f4b-cc40-e053-6394a90a873e2026-06-30Warnings, Adverse reactionsExact identifier
rxcui: 313988
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEREMEDYREPACK INC.916de29e-228c-4dfc-bcee-ad9a641316bd2026-06-24Warnings, Adverse reactionsExact identifier
rxcui: 313988
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEREMEDYREPACK INC.e8c27f1c-dc81-44b1-8663-a7d663bad89f2026-06-23Warnings, Adverse reactionsExact identifier
rxcui: 310429
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEAtlantic Biologicals Corp.54ed0dd9-2fa8-269a-e063-6294a90a607c2026-06-23Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FUROSEMIDEFUROSEMIDEHF Acquisition Co LLC, DBA HealthFirst75d5611a-f9e0-1841-e053-2991aa0af4152026-06-23Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEUnit Dose Solutions, Inc.54dd664a-c7ec-27f3-e063-6294a90aff9f2026-06-22Warnings, Adverse reactionsExact identifier
rxcui: 310429
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDECardinal Health 107, LLC2a5bcf50-6d63-463a-915e-a72ea2e5f1312026-06-18Warnings, Adverse reactionsExact identifier
application number: ANDA076796
ndc (package): 55154-2348-0
ndc (package): 55154-2349-0
ndc (product): 55154-2348
ndc (product): 55154-2349
ndc11 (package): 55154234800
rxcui: 313988
rxcui: 310429
spl id: a95b8b66-b866-4dfb-a05f-186616d93f56
spl set id: 2a5bcf50-6d63-463a-915e-a72ea2e5f131
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEGranulation Technology, Inc.462e8917-cbe0-f4f9-e063-6394a90ab4ff2026-06-17Warnings, Adverse reactionsExact identifier
rxcui: 313988
rxcui: 310429
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEAtlantic Biologicals Corps9c342198-7162-4cc5-bda1-bc4054a4292b2026-06-16Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDECoupler LLC53e58232-f7f9-c09b-e063-6394a90a5bc42026-06-10Warnings, Adverse reactionsExact identifier
rxcui: 310429
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDECardinal Health 107, LLC42478c55-9056-487a-89a9-d36904beea122026-06-02Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEMajor Pharmaceuticals6be1addd-a811-47fc-8650-6870d661c2342026-05-26Warnings, Adverse reactionsExact identifier
application number: ANDA076796
ndc (product): 0904-7177
ndc (product): 0904-7178
rxcui: 313988
rxcui: 310429
spl id: ee764e1d-0e34-4e02-bab5-c766786f7663
spl set id: 6be1addd-a811-47fc-8650-6870d661c234
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDECardinal Health 107, LLC71b48f4d-9936-448c-9e3a-33f1182e10392026-05-15Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEHospira, Inc.39fd32f2-6bb7-4a65-d298-e48d26bc80c72026-05-13Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5

Reported adverse events (FAERS/openFDA)#

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