NDC 70518-3061-7 - 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
70518-3061
Requested NDC
70518-3061-7
Package NDCs from labels
70518-3061-0, 70518-3061-1, 70518-3061-2, 70518-3061-3, 70518-3061-4, 70518-3061-5, 70518-3061-7, 70518-3061-6
Manufacturer
REMEDYREPACK INC.
Effective date
2026-07-15
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 mgREMEDYREPACK INC.2026-07-15HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70518-3061-0Furosemide5 in 1 BOTTLE, PLASTICTABLET513
70518-3061-1Furosemide30 in 1 BLISTER PACKTABLET3013
70518-3061-2Furosemide30 in 1 BLISTER PACKTABLET3013
70518-3061-3Furosemide30 in 1 BOTTLE, PLASTICTABLET3013
70518-3061-4Furosemide14 in 1 BOTTLE, PLASTICTABLET1413
70518-3061-5Furosemide7 in 1 BOTTLE, PLASTICTABLET713
70518-3061-6Furosemide50 in 1 BOXTABLET5013
70518-3061-7Furosemide1 in 1 POUCHTABLET113

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70518-3061FUROSEMIDE TABLET [REMEDYREPACK INC.]8Current NDC, Legacy NDC, 8 package rows20250104_3d312ab0-589c-427b-84da-18887244bfc9.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.