FDA.reportPublic FDA data

NDC 68071-4445-01 - 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
68071-4445
Requested NDC
68071-4445-01
Package NDCs from labels
68071-4445-1, 68071-4445-2, 68071-4445-3, 68071-4445-4, 68071-4445-6, 68071-4445-9, 68071-4445-8, 68071-4445-01
Manufacturer
NuCare Pharmaceuticals,Inc.
Effective date
2024-06-10
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
FUROSEMIDE TABLETS, USP 20, 40, and 80 mgNuCare Pharmaceuticals,Inc.2024-06-10HUMAN PRESCRIPTION DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDCEffectiveRelated label
68071-4445-12023-04-17FUROSEMIDE TABLETS, USP 20, 40, and 80 mg
68071-4445-22023-04-17FUROSEMIDE TABLETS, USP 20, 40, and 80 mg
68071-4445-32023-04-17FUROSEMIDE TABLETS, USP 20, 40, and 80 mg
68071-4445-42023-04-17FUROSEMIDE TABLETS, USP 20, 40, and 80 mg
68071-4445-62023-04-17FUROSEMIDE TABLETS, USP 20, 40, and 80 mg
68071-4445-82023-04-17FUROSEMIDE TABLETS, USP 20, 40, and 80 mg
68071-4445-92023-04-17FUROSEMIDE TABLETS, USP 20, 40, and 80 mg
68071-4445-12023-01-30FUROSEMIDE TABLETS, USP 20, 40, and 80 mg
68071-4445-22023-01-30FUROSEMIDE TABLETS, USP 20, 40, and 80 mg
68071-4445-32023-01-30FUROSEMIDE TABLETS, USP 20, 40, and 80 mg
68071-4445-42023-01-30FUROSEMIDE TABLETS, USP 20, 40, and 80 mg
68071-4445-62023-01-30FUROSEMIDE TABLETS, USP 20, 40, and 80 mg
68071-4445-82023-01-30FUROSEMIDE TABLETS, USP 20, 40, and 80 mg
68071-4445-92023-01-30FUROSEMIDE TABLETS, USP 20, 40, and 80 mg
68071-4445-12021-02-16FUROSEMIDE TABLETS, USP 20, 40, and 80 mg
68071-4445-22021-02-16FUROSEMIDE TABLETS, USP 20, 40, and 80 mg
68071-4445-32021-02-16FUROSEMIDE TABLETS, USP 20, 40, and 80 mg
68071-4445-42021-02-16FUROSEMIDE TABLETS, USP 20, 40, and 80 mg
68071-4445-62021-02-16FUROSEMIDE TABLETS, USP 20, 40, and 80 mg
68071-4445-82021-02-16FUROSEMIDE TABLETS, USP 20, 40, and 80 mg
68071-4445-92021-02-16FUROSEMIDE TABLETS, USP 20, 40, and 80 mg
68071-4445-12021-01-29FUROSEMIDE TABLETS, USP 20, 40, and 80 mg
68071-4445-22021-01-29FUROSEMIDE TABLETS, USP 20, 40, and 80 mg
68071-4445-32021-01-29FUROSEMIDE TABLETS, USP 20, 40, and 80 mg
68071-4445-42021-01-29FUROSEMIDE TABLETS, USP 20, 40, and 80 mg
68071-4445-62021-01-29FUROSEMIDE TABLETS, USP 20, 40, and 80 mg
68071-4445-82021-01-29FUROSEMIDE TABLETS, USP 20, 40, and 80 mg
68071-4445-92021-01-29FUROSEMIDE TABLETS, USP 20, 40, and 80 mg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68071-4445-1Furosemide10 in 1 BOTTLETABLET105
68071-4445-2Furosemide20 in 1 BOTTLETABLET205
68071-4445-3Furosemide30 in 1 BOTTLETABLET305
68071-4445-4Furosemide40 in 1 BOTTLETABLET405
68071-4445-6Furosemide60 in 1 BOTTLETABLET605
68071-4445-8Furosemide180 in 1 BOTTLETABLET1805
68071-4445-9Furosemide90 in 1 BOTTLETABLET905

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68071-4445FUROSEMIDE TABLET [NUCARE PHARMACEUTICALS,INC.]5Current NDC, Legacy NDC, 7 package rows20240612_6cbf3834-0433-4dc0-e053-2a91aa0a8f8a.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 2 of 8 · 157 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
rxcui: 313988
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEPreferred Pharmaceuticals Inc.cad102d7-0197-4cff-bb80-9f0b5bcb599b2026-04-29Warnings, Adverse reactionsExact identifier
rxcui: 310429
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEREMEDYREPACK INC.7181e528-c862-4dd7-8446-9011e4c7312a2026-04-23Warnings, Adverse reactionsExact identifier
application number: ANDA076796
rxcui: 313988
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
rxcui: 310429
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
rxcui: 313988
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEDirect_Rxe9be5c3b-4b18-7ad2-e053-2995a90a4a8b2026-03-09Warnings, Adverse reactionsExact identifier
rxcui: 313988
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEMarlex Pharmaceuticals, Inc.4bd1b15e-354e-051f-e063-6294a90a3f3b2026-03-01Warnings, Adverse reactionsExact identifier
rxcui: 313988
rxcui: 197732
rxcui: 310429
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDENuCare Pharmaceuticals,Inc.bd45c963-a413-e9a1-e053-2a95a90a14382026-02-19Warnings, Adverse reactionsExact identifier
application number: ANDA076796
rxcui: 313988
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEPreferred Pharmaceuticals Inc.adda78ee-0cf5-4613-a748-5d6571afe3542026-01-19Warnings, Adverse reactionsExact identifier
rxcui: 313988
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
application number: ANDA076796
rxcui: 313988
rxcui: 197732
rxcui: 310429
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
rxcui: 313988
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.