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 3 of 8 · 157 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
FurosemideFUROSEMIDEPhlow Corporation08a44bdd-028d-41af-9d4e-70971b0bcc4e2026-01-09Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDENorthwind Health Company, LLC13ba97a7-598a-76a4-e063-6294a90a45c52026-01-02Warnings, Adverse reactionsExact identifier
rxcui: 310429
unii: 7LXU5N7ZO5
FUROSEMIDEFUROSEMIDENorthwind Health Company, LLC1d99e151-75ba-6a75-e063-6294a90a43602026-01-01Warnings, Adverse reactionsExact identifier
rxcui: 313988
rxcui: 310429
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDENorthwind Health Company, LLCf2b920b2-f8b3-1e6e-e053-2a95a90ae1532026-01-01Warnings, Adverse reactionsExact identifier
application number: ANDA076796
rxcui: 310429
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDENorthwind Health Company, LLCf3173c0d-2b62-7c7b-e053-2995a90ada052026-01-01Warnings, Adverse reactionsExact identifier
rxcui: 310429
unii: 7LXU5N7ZO5
Medicated Cornstarch Baby PowderACTIVE CORN STARCHDavion, Inc.e39032d1-c8cd-4a41-af10-126970b8ad382025-12-29WarningsExact identifier
unii: O8232NY3SJ
FurosemideFUROSEMIDERedpharm Drug3745be12-ea1d-f450-e063-6294a90a148c2025-12-24Warnings, Adverse reactionsExact identifier
rxcui: 313988
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEProPharma Distribution38550de1-f099-0cdf-e063-6294a90a9e262025-12-18Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEA-S Medication Solutions54a33042-a163-4f93-96cc-fbd93030e0142025-12-05Warnings, Adverse reactionsExact identifier
rxcui: 310429
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEA-S Medication Solutions6864b3f6-c5ad-4588-ad04-5260258c6d8c2025-12-05Warnings, Adverse reactionsExact identifier
rxcui: 310429
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEQPharma Inc341e29d9-a6f1-4c77-ae44-9b2c423ea6b42025-12-03Warnings, Adverse reactionsExact identifier
rxcui: 313988
unii: 7LXU5N7ZO5
LASIX ONYUFUROSEMIDESQ Innovation, Inc.cb27654f-c7a1-4796-ab08-60a5fa16f5c02025-11-14Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FUROSEMIDEFUROSEMIDECivica, Inc.7ecaa5af-d186-4380-b105-e7e528f75cc72025-11-12Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEEugia US LLC421aa6d5-623b-4dc2-abd5-bb9e7765bf372025-11-11Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEProPharma Distribution43053bf7-9050-dba8-e063-6294a90a71742025-11-07Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEHikma Pharmaceuticals USA Inc.9e493331-dddd-496e-abf8-61747fb67aba2025-11-03Warnings, Adverse reactionsExact identifier
rxcui: 313988
rxcui: 197732
rxcui: 310429
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDECivica, Inc.6d9caaab-d874-4cf1-b9fe-408452a189982025-10-31Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FUROSEMIDEFUROSEMIDEHenry Schein, Inc.a9853417-0442-4f53-9543-e0749bc3c80d2025-10-31Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEHenry Schein, Inc.d8407b0e-7838-4ab6-b9dd-1f7ecf1e0a172025-10-31Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FUROSEMIDEFUROSEMIDEHenry Schein, Inc.15e4c3a3-7d64-471e-bfdf-6156731e24aa2025-10-31Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5

Reported adverse events (FAERS/openFDA)#

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