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 8 of 8 · 157 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
FurosemideFUROSEMIDEBryant Ranch Prepack01a5f094-b473-4e46-9e61-69d5ec6dd7662023-03-01Warnings, Adverse reactionsExact identifier
application number: ANDA076796
rxcui: 197732
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEBryant Ranch Prepack6820724c-1ca5-451c-9d2b-2d38e60036f52023-03-01Warnings, Adverse reactionsExact identifier
application number: ANDA076796
rxcui: 313988
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEBryant Ranch Prepack440aaaed-47df-4bb5-8b41-2c80568936792023-03-01Warnings, Adverse reactionsExact identifier
application number: ANDA076796
rxcui: 313988
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEBryant Ranch Prepack15ae6f44-88dd-4455-b1f7-4718c91e7b662023-03-01Warnings, Adverse reactionsExact identifier
application number: ANDA076796
rxcui: 197732
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEBryant Ranch Prepack3ad12e70-3c2e-44af-bb6b-5762d181c76b2023-03-01Warnings, Adverse reactionsExact identifier
application number: ANDA076796
rxcui: 310429
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEA-S Medication Solutions52f0c9d5-396f-4033-abe8-145eec3e69832023-02-06Warnings, Adverse reactionsExact identifier
rxcui: 310429
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDELifestar Pharma LLC92f3ab5d-361c-4e12-bb50-fd4a9f195a8f2022-12-22Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEProficient Rx LP595ddaf2-c2cb-44a4-a46c-53bcfe6bd7522022-12-01Warnings, Adverse reactionsExact identifier
rxcui: 310429
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDESagent Pharmaceuticalsd63c1277-dd7e-4d21-9e80-68143f55e2dc2022-11-29Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDELeading Pharma, LLCb5c6fcf4-fd37-4fee-8dac-1a3273d95ffe2022-11-11Warnings, Adverse reactionsExact identifier
rxcui: 313988
rxcui: 197732
rxcui: 310429
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEPrecision Dose Inc.4a746634-379b-4847-a965-7607d2a71bed2022-09-21Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEAphena Pharma Solutions - Tennessee, LLC6f124d7d-a19d-4de6-8ea4-719a42eb520b2022-03-10Warnings, Adverse reactionsExact identifier
application number: ANDA076796
rxcui: 313988
rxcui: 197732
rxcui: 310429
unii: 7LXU5N7ZO5
FUROSEMIDEFUROSEMIDEHF Acquisition Co LLC, DBA HealthFirstc5d9b063-e3fe-ec2f-e053-2995a90ab3f22021-06-28Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEProficient Rx LPce84359c-2f76-421a-9b2b-79b1c2be2f202021-01-01Warnings, Adverse reactionsExact identifier
rxcui: 313988
rxcui: 310429
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEGland Pharma Limited644704c0-e6a5-4804-bfa6-795c8f83aa7a2020-07-03Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEAphena Pharma Solutions - Tennessee, LLC1d2733ac-6fa6-44d1-96d4-f1a698045ad22018-04-18Warnings, Adverse reactionsExact identifier
application number: ANDA076796
rxcui: 313988
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEAphena Pharma Solutions - Tennessee, LLC6fbf7f3d-7566-44d5-9507-c4460238fc912018-02-09Warnings, Adverse reactionsExact identifier
rxcui: 313988
rxcui: 310429
unii: 7LXU5N7ZO5

Reported adverse events (FAERS/openFDA)#

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