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 6 of 8 · 157 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
FurosemideFUROSEMIDENuCare Pharmaceuticals,Inc.809d9734-12dd-3b1f-e053-2a91aa0aadee2025-01-02Warnings, Adverse reactionsExact identifier
rxcui: 313988
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDENuCare Pharmaceuticals,Inc.813c8e9b-61bc-27c4-e053-2a91aa0a9f452024-12-26Warnings, Adverse reactionsExact identifier
rxcui: 310429
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEFresenius Kabi USA, LLCc794c95a-654e-48fe-9596-201fc122ff752024-12-09Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEFresenius Kabi USA, LLC3747bbcd-783d-4baa-bb5b-b6827bf390e32024-12-09Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FUROSEMIDEFUROSEMIDEDevatis Inc.c90bcb14-eb8d-4753-b339-3469c664ecd22024-10-31Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDENCS HealthCare of KY, LLC dba Vangard Labs114f4f4f-536a-4658-8fd0-2dd8c029b19a2024-09-17Warnings, Adverse reactionsExact identifier
application number: ANDA076796
rxcui: 313988
rxcui: 197732
rxcui: 310429
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEBryant Ranch Prepack25c0aded-ffcd-4145-a48c-76c5fb220f612024-08-23Warnings, Adverse reactionsExact identifier
application number: ANDA076796
rxcui: 313988
rxcui: 310429
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEBryant Ranch Prepack0dd28e18-2e15-45eb-9a61-a9de7bd7d64e2024-08-23Warnings, Adverse reactionsExact identifier
rxcui: 310429
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDENuCare Pharmaceuticals,Inc.809b4f68-4fca-c201-e053-2a91aa0ac18e2024-07-15Warnings, Adverse reactionsExact identifier
rxcui: 313988
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEAccord Healthcare, Inc.f6f64972-714c-4ee9-8a5e-9ffcab41a73b2024-07-11Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEAphena Pharma Solutions - Tennessee, LLC307c3b89-f37f-45ee-8ec7-d402008cf2fa2024-06-28Warnings, Adverse reactionsExact identifier
rxcui: 310429
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEPrecision Dose Inc.3fd02fb5-98a0-4eda-a0ec-41faabe047062024-06-13Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDENuCare Pharmaceuticals,Inc.6cbf3834-0433-4dc0-e053-2a91aa0a8f8a2024-06-10Warnings, Adverse reactionsExact identifier
application number: ANDA076796
ndc (package): 68071-4445-3
ndc (package): 68071-4445-1
ndc (package): 68071-4445-8
ndc (package): 68071-4445-6
ndc (package): 68071-4445-4
ndc (package): 68071-4445-9
ndc (package): 68071-4445-2
ndc (product): 68071-4445
ndc11 (package): 68071444501
rxcui: 313988
spl id: 1a8ce174-9cb5-77f8-e063-6394a90ae5b2
spl set id: 6cbf3834-0433-4dc0-e053-2a91aa0a8f8a
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDENuCare Pharmaceuticals,Inc.7316929d-413a-e78f-e053-2a91aa0a417e2024-06-10Warnings, Adverse reactionsExact identifier
application number: ANDA076796
rxcui: 313988
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDENuCare Pharmaceuticals,Inc.73e5c8f3-32f8-114c-e053-2a91aa0ab5002024-06-10Warnings, Adverse reactionsExact identifier
application number: ANDA076796
rxcui: 310429
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEAphena Pharma Solutions - Tennessee, LLC4b3e2e13-a657-4da5-b536-8ae0a26812e02024-06-03Warnings, Adverse reactionsExact identifier
application number: ANDA076796
rxcui: 310429
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEA-S Medication Solutions83662449-f2b1-48a3-9021-13037e64e6ea2024-04-23Warnings, Adverse reactionsExact identifier
rxcui: 313988
rxcui: 197732
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDECalvin Scott & Co., Inc.b2cc89e5-6619-4113-ad31-48076652c8562024-04-18Warnings, Adverse reactionsExact identifier
rxcui: 313988
unii: 7LXU5N7ZO5
Pure Cornstarch BabyCORN STARCHWalgreen Companyd0e9bd13-b568-4f7e-b036-8d23e71ad8bf2024-03-25WarningsExact identifier
unii: O8232NY3SJ
FurosemideFUROSEMIDEBryant Ranch Prepack3b028a3c-102a-40f1-820e-b187ff1e18032024-03-22Warnings, Adverse reactionsExact identifier
application number: ANDA076796
rxcui: 310429
unii: 7LXU5N7ZO5

Reported adverse events (FAERS/openFDA)#

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