NDC 72162-1360-01 - 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
72162-1360
Requested NDC
72162-1360-01
Package NDCs from labels
72162-1360-1, 72162-1360-0, 72162-1360-01
Manufacturer
Bryant Ranch Prepack
Effective date
2024-02-02
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 Prepack2024-02-02HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72162-1360-0Furosemide1000 in 1 BOTTLE, PLASTICTABLET1000100
72162-1360-1Furosemide100 in 1 BOTTLE, PLASTICTABLET100100

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72162-1360FUROSEMIDE TABLET [BRYANT RANCH PREPACK]100Current NDC, 2 package rows20240203_d07ff11c-c1ab-41e6-a455-f2b89340106e.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
72162-1360-0EA - Each72162-1360c1745eeb-70ff-4582-8bb9-92625c4ea79d12024-03-12
72162-1360-1EA - Each72162-1360f7d568d5-a3e3-4693-ad64-369d38ec796c12024-03-12

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 5 of 8 · 157 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
FUROSEMIDEFUROSEMIDEAurobindo Pharma Limiteda504ee4b-3995-45f2-898c-91116dd81d192025-07-19Warnings, Adverse reactionsExact identifier
rxcui: 313988
rxcui: 197732
rxcui: 310429
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEPD-Rx Pharmaceuticals, Inc.3ba730ab-90d4-478a-80b3-1ea3edb03e4d2025-07-15Warnings, Adverse reactionsExact identifier
application number: ANDA076796
rxcui: 310429
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDENorthStar Rx LLCfc3194a3-7e75-4551-8334-4a5cc22d9f8b2025-07-07Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEProficient Rx LP600ca175-be2b-4c43-b119-133ae21a56012025-07-01Warnings, Adverse reactionsExact identifier
rxcui: 313988
unii: 7LXU5N7ZO5
FUROSEMIDEFUROSEMIDEBaxter Healthcare Corporationc71371a7-75c5-45b8-b762-8d782d4c71bc2025-06-30Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDESagent Pharmaceuticalsd76bd85a-8e57-477e-9607-c9435f1e26fb2025-06-26Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
Steritalc 2gTALCNovatech SAc94e51d9-beef-4b06-e053-2a95a90a754a2025-06-25Warnings, Adverse reactionsExact identifier
unii: 7SEV7J4R1U
FurosemideFUROSEMIDESolco Healthcare LLC6a0fb397-63ae-4fce-bddf-16a91b1b7a2f2025-06-18Warnings, Adverse reactionsExact identifier
application number: ANDA076796
ndc (product): 43547-401
rxcui: 313988
rxcui: 197732
rxcui: 310429
spl id: f49380e9-82e1-439c-8cef-668d44a8e1ca
spl set id: 6a0fb397-63ae-4fce-bddf-16a91b1b7a2f
unii: 7LXU5N7ZO5
SENSITIVE POCKET SUNSENSITIVE POCKET SUNShantou Oushiya Biotechnology Co., Ltd36ac412f-e31f-6906-e063-6394a90a4a3d2025-06-14WarningsExact identifier
unii: 7SEV7J4R1U
FurosemideFUROSEMIDEMaiva Pharma Private Limitede5880bf4-5037-4813-b7cc-656a6832ecb52025-06-13WarningsExact identifier
unii: 7LXU5N7ZO5
UDSxMP Medicated SystemFUROSEMIDE, BENZALKONIUM CHLORIDEWellbeing Medical Supply06b901dc-0f1d-424f-8c4b-a29113cbab252025-06-12Warnings, Adverse reactionsExact identifier
rxcui: 310429
UDSx Medicated SystemFUROSEMIDE, BENZALKONIUM CHLORIDEWellbeing Medical Supply8f1df75b-101a-45da-924a-2767c34a4efe2025-06-12Warnings, Adverse reactionsExact identifier
rxcui: 310429
FurosemideFUROSEMIDEPrefferred Pharmaceuticals Inc.ede9846b-b4c5-4be2-9188-fd65e66cd8932025-04-30Warnings, Adverse reactionsExact identifier
rxcui: 310429
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDECoupler LLC33ec71e2-8fbd-0703-e063-6294a90a62e12025-04-29Warnings, Adverse reactionsExact identifier
rxcui: 197732
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEChartwell RX, LLC8ebd2f10-acfc-48a4-a5db-f20377bda9ce2025-03-26Warnings, Adverse reactionsExact identifier
rxcui: 313988
rxcui: 310429
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEHikma Pharmaceuticals USA Inc.ddfc41a9-37d4-49c1-bbf3-969a98cd649c2025-03-10Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEAvenacy Inc.7d0db0f7-bf4f-4b0b-9359-2a838626e04b2025-02-28Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDERising Pharma Holdings, Inc.6101b9b4-f3ef-438e-a857-b4ea55ffc6792025-02-21Warnings, Adverse reactionsExact identifier
rxcui: 313988
rxcui: 197732
rxcui: 310429
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDECamber Pharmaceuticals, Inc.f6221cce-e586-4002-bd14-6ec22eb14e2e2025-01-30Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 7LXU5N7ZO5
FurosemideFUROSEMIDEIpca Laboratories Limited0acd293b-ecab-4879-a8e7-cd1b76148f2a2025-01-20Warnings, Adverse reactionsExact identifier
rxcui: 313988
rxcui: 197732
rxcui: 310429
unii: 7LXU5N7ZO5

Reported adverse events (FAERS/openFDA)#

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