FDA.reportPublic FDA data

NDC 72162-1361-00 - 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
72162-1361
Requested NDC
72162-1361-00
Package NDCs from labels
72162-1361-0, 72162-1361-1, 72162-1361-00
Manufacturer
Bryant Ranch Prepack
Effective date
2023-10-04
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Furosemide - Bryant Ranch PrepackBryant Ranch Prepack2023-10-04HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72162-1361-0Furosemide1000 in 1 BOTTLE, PLASTICTABLET1000100
72162-1361-1Furosemide100 in 1 BOTTLE, PLASTICTABLET100100

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72162-1361FUROSEMIDE TABLET [BRYANT RANCH PREPACK]100Current NDC, 2 package rows20231005_020bc039-9e99-4895-96f8-0c6a556d3e67.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
72162-1361-0EA - Each72162-136158bf699f-f7d3-4855-a47e-b65f0fcd842312023-12-05
72162-1361-1EA - Each72162-1361d363da08-f279-43fc-bfe3-1a630e7e803e12023-12-05

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 1 of 8 · 157 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
FurosemideFUROSEMIDEREMEDYREPACK INC.dba00759-87b4-4ecf-998e-ba03ed3d2f1a2026-08-17Warnings, Adverse reactionsExact identifier
rxcui: 310429
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDERedpharm Drug58d2a38d-75f8-dcb9-e063-6294a90a10d72026-08-12Warnings, Adverse reactionsExact identifier
rxcui: 310429
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEMedical Purchasing Solutions, LLC58cc1e38-6000-1489-e063-6394a90a59782026-08-11Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FUROSCIXFUROSEMIDE INJECTION 80 MG/ 10 MLscPharmaceuticals Inc., a wholly owned subsidiary of MannKind Corporationeac958dd-8d43-e44e-e053-2995a90a4d5e2026-07-31Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEREMEDYREPACK INC.7cdcd001-ab4b-4210-a455-2e17a7bc49722026-07-24Warnings, Adverse reactionsExact identifier
rxcui: 310429
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEREMEDYREPACK INC.3d312ab0-589c-427b-84da-18887244bfc92026-07-15Warnings, Adverse reactionsExact identifier
application number: ANDA076796
rxcui: 310429
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDESt. Mary's Medical Park Pharmacyfebeaf8c-0f4b-cc40-e053-6394a90a873e2026-06-30Warnings, Adverse reactionsExact identifier
rxcui: 313988
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEREMEDYREPACK INC.916de29e-228c-4dfc-bcee-ad9a641316bd2026-06-24Warnings, Adverse reactionsExact identifier
rxcui: 313988
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEREMEDYREPACK INC.e8c27f1c-dc81-44b1-8663-a7d663bad89f2026-06-23Warnings, Adverse reactionsExact identifier
rxcui: 310429
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEAtlantic Biologicals Corp.54ed0dd9-2fa8-269a-e063-6294a90a607c2026-06-23Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FUROSEMIDEFUROSEMIDEHF Acquisition Co LLC, DBA HealthFirst75d5611a-f9e0-1841-e053-2991aa0af4152026-06-23Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEUnit Dose Solutions, Inc.54dd664a-c7ec-27f3-e063-6294a90aff9f2026-06-22Warnings, Adverse reactionsExact identifier
rxcui: 310429
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDECardinal Health 107, LLC2a5bcf50-6d63-463a-915e-a72ea2e5f1312026-06-18Warnings, Adverse reactionsExact identifier
application number: ANDA076796
rxcui: 313988
rxcui: 310429
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEGranulation Technology, Inc.462e8917-cbe0-f4f9-e063-6394a90ab4ff2026-06-17Warnings, Adverse reactionsExact identifier
rxcui: 313988
rxcui: 197732
rxcui: 310429
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEAtlantic Biologicals Corps9c342198-7162-4cc5-bda1-bc4054a4292b2026-06-16Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDECoupler LLC53e58232-f7f9-c09b-e063-6394a90a5bc42026-06-10Warnings, Adverse reactionsExact identifier
rxcui: 310429
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDECardinal Health 107, LLC42478c55-9056-487a-89a9-d36904beea122026-06-02Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEMajor Pharmaceuticals6be1addd-a811-47fc-8650-6870d661c2342026-05-26Warnings, Adverse reactionsExact identifier
application number: ANDA076796
rxcui: 313988
rxcui: 310429
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDECardinal Health 107, LLC71b48f4d-9936-448c-9e3a-33f1182e10392026-05-15Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEHospira, Inc.39fd32f2-6bb7-4a65-d298-e48d26bc80c72026-05-13Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5

Reported adverse events (FAERS/openFDA)#

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