Home NDC 63323-280-01 NDC 63323-280-01 - 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 63323-280
Requested NDC 63323-280-01
Package NDCs from labels 63323-280-01, 63323-280-02, 63323-280-03, 63323-280-04, 63323-280-05, 63323-280-10, 63323-280-41, 63323-280-16, 63323-280-43, 63323-280-26, 63323-280-45, 63323-280-36
Manufacturer Cardinal Health 107, LLC
Effective date 2026-06-02
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Furosemide - Cardinal Health 107, LLC Cardinal Health 107, LLC 2026-06-02 HUMAN PRESCRIPTION DRUG LABEL Furosemide - Cardinal Health 107, LLC Cardinal Health 107, LLC 2025-10-03 HUMAN PRESCRIPTION DRUG LABEL Furosemide - Fresenius Kabi USA, LLC Fresenius Kabi USA, LLC 2024-12-09 HUMAN PRESCRIPTION DRUG LABEL Furosemide - Fresenius Kabi USA, LLC Fresenius Kabi USA, LLC 2024-12-09 HUMAN PRESCRIPTION DRUG LABEL FUROSEMIDE - HF Acquisition Co LLC, DBA HealthFirst HF Acquisition Co LLC, DBA HealthFirst 2024-01-28 HUMAN PRESCRIPTION DRUG LABEL FUROSEMIDE - HF Acquisition Co LLC, DBA HealthFirst HF Acquisition Co LLC, DBA HealthFirst 2024-01-22 HUMAN PRESCRIPTION DRUG LABEL FUROSEMIDE - HF Acquisition Co LLC, DBA HealthFirst HF Acquisition Co LLC, DBA HealthFirst 2021-06-28 HUMAN PRESCRIPTION DRUG LABEL Model AA-8565CV-ACT Model AA-8565CV - Aerospace Accessory Service, Inc Aerospace Accessory Service, Inc 2021-05-18 MEDICAL DEVICE
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63323-280-01 Furosemide 2 mL in 1 VIAL INJECTION, SOLUTION 2 6 63323-280-02 Furosemide 25 in 1 TRAY INJECTION, SOLUTION 25 6 63323-280-03 Furosemide 4 mL in 1 VIAL INJECTION, SOLUTION 4 6 63323-280-04 Furosemide 25 in 1 TRAY INJECTION, SOLUTION 25 6 63323-280-05 Furosemide 10 mL in 1 VIAL INJECTION, SOLUTION 10 6 63323-280-10 Furosemide 25 in 1 TRAY INJECTION, SOLUTION 25 6 63323-280-16 Furosemide 25 in 1 TRAY INJECTION, SOLUTION 25 5 63323-280-26 Furosemide 25 in 1 TRAY INJECTION, SOLUTION 25 5 63323-280-36 Furosemide 25 in 1 TRAY INJECTION, SOLUTION 25 5 63323-280-41 Furosemide 2 mL in 1 VIAL INJECTION, SOLUTION 2 5 63323-280-43 Furosemide 4 mL in 1 VIAL INJECTION, SOLUTION 4 5 63323-280-45 Furosemide 10 mL in 1 VIAL INJECTION, SOLUTION 10 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 63323-280 FUROSEMIDE INJECTION, SOLUTION [FRESENIUS KABI USA, LLC] 6 Current NDC, Legacy NDC, 6 package rows 20241222_c794c95a-654e-48fe-9596-201fc122ff75.zip 63323-280 FUROSEMIDE INJECTION, SOLUTION [FRESENIUS KABI USA, LLC] 5 Current NDC, Legacy NDC, 6 package rows 20241222_3747bbcd-783d-4baa-bb5b-b6827bf390e3.zip
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded FUROSEMIDE ACTIVE INGREDIENT 7LXU5N7ZO5 FUROSEMIDE INJECTION, SOLUTION [APP PHARMACEUTICALS, LLC] 1 FUROSEMIDE ACTIVE MOIETY 7LXU5N7ZO5 FUROSEMIDE INJECTION, SOLUTION [APP PHARMACEUTICALS, LLC] 1 HYDROCHLORIC ACID INACTIVE INGREDIENT QTT17582CB FUROSEMIDE INJECTION, SOLUTION [APP PHARMACEUTICALS, LLC] 1 SODIUM CHLORIDE INACTIVE INGREDIENT 451W47IQ8X FUROSEMIDE INJECTION, SOLUTION [APP PHARMACEUTICALS, LLC] 1 SODIUM HYDROXIDE INACTIVE INGREDIENT 55X04QC32I FUROSEMIDE INJECTION, SOLUTION [APP PHARMACEUTICALS, LLC] 1
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 53 of 733 · 14,654 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Calmco Allergy Relief DIPHENHYDRAMINE HCL CalmCo LLC 471b1a43-1708-8be7-e063-6394a90a9bb7 2026-07-06 Warnings Exact identifier unii: TC2D6JAD40 Dr Kids Pain and Fever ACETAMINOPHEN CalmCo LLC 2ee6df99-727a-34c6-e063-6294a90a6bbc 2026-07-06 Warnings Exact identifier unii: 362O9ITL9D Dr Kids Allergy Relief DIPHENHYDRAMINE HCL CalmCo LLC 28ec213e-fabb-28ec-e063-6394a90ad102 2026-07-06 Warnings Exact identifier unii: TC2D6JAD40 Promethazine Hydrochloride PROMETHAZINE HYDROCHLORIDE Coupler LLC 55f618d1-4466-3200-e063-6394a90a89a8 2026-07-06 Boxed warning, Warnings, Adverse reactions Exact identifier unii: R61ZEH7I1I Aspirin ASPIRIN Trifecta Pharmaceuticals USA LLC 227cefca-acc4-41d0-e063-6394a90a35b9 2026-07-06 Warnings Exact identifier unii: R16CO5Y76E Premier Tinted Mineral Sunscreen BROAD SPECTRUM SPF30 Emerald Aesthetics LLC 55f88dd1-346c-22a5-e063-6294a90a711f 2026-07-06 Warnings Exact identifier unii: 15FIX9V2JP Hand Sanitizer ETHYL ALCOHOL EverywhereAire LLC b48f9e6b-c616-3607-e053-2995a90a37f5 2026-07-06 Warnings Exact identifier application number: M003 unii: 3K9958V90M PlaneAire Hands hand sanitizer ETHYL ALCOHOL EverywhereAire LLC b6af3009-78c2-2312-e053-2995a90af90a 2026-07-06 Warnings Exact identifier application number: M003 unii: 3K9958V90M Hand Sanitizer gel ALCOHOL EverywhereAire LLC d2a6c866-3f1e-20f1-e053-2995a90a26cc 2026-07-06 Warnings Exact identifier application number: M003 unii: 3K9958V90M PlaneAire Hands HAND SANITIZER ETHANOL-BASED EverywhereAire LLC eab3ab67-cb27-6c2b-e053-2a95a90ace12 2026-07-06 Warnings Exact identifier application number: M003 unii: 3K9958V90M PlaneAire Hands Sandalwood ETHANOL HAND SANITIZER EverywhereAire LLC 18612a10-8667-b0ef-e063-6394a90a208e 2026-07-06 Warnings Exact identifier application number: M003 unii: 3K9958V90M PlaneAire Hands ETHANOL HAND SANITIZER EverywhereAire LLC b86824c2-4fae-d597-e053-2995a90ad1da 2026-07-06 Warnings Exact identifier application number: M003 unii: 3K9958V90M PlaneAire Hands Lemon Olive Oil Hand Sanitizer ETHANOL HAND SANITIZER EverywhereAire LLC 42f8c2fb-a4e6-9416-e063-6294a90af9d5 2026-07-06 Warnings Exact identifier application number: M003 unii: 3K9958V90M Extra Strength Pain Aid ACETAMINOPHEN, ASPIRIN, CAFFEINE Hi-Tech Nutaceuticals, LLC a39e4b99-700d-0f5c-e053-2a95a90a6bd3 2026-07-06 Warnings Exact identifier unii: R16CO5Y76E unii: 362O9ITL9D Nighttime Sleep Aid ACETAMINOPHEN, DIPHENHYDRAMINE Hi-Tech Nutraceuticals, LLC a39e2bd6-3d0a-642b-e053-2995a90a42a0 2026-07-06 Warnings Exact identifier unii: TC2D6JAD40 unii: 362O9ITL9D PlaneAire Hands HAND SANITIZER ETHANOL BASED EverywhereAire LLc eab52ae1-f588-b08b-e053-2995a90a96b2 2026-07-06 Warnings Exact identifier application number: M003 unii: 3K9958V90M PlaneAire Hands hand sanitizer HAND SANITIZER ETHANOL-BASED EverywhereAire LLC eab19649-21fc-2fa4-e053-2995a90a90f9 2026-07-06 Warnings Exact identifier application number: M003 unii: 3K9958V90M Extra Strength Acetaminophen ACETAMINOPHEN Hi-Tech Nutraceuticals, LLC a36be487-7a36-550f-e053-2a95a90a95c1 2026-07-06 Warnings Exact identifier unii: 362O9ITL9D Acetaminophen ACETAMINOPHEN Hi-Tech Nutraceuticals, LLC a39c524e-c131-d7fb-e053-2995a90a785b 2026-07-06 Warnings Exact identifier unii: 362O9ITL9D Theraflu Severe Cold Relief Daytime ACETAMINOPHEN, DEXTROMETHORPHAN HBR Select Consumer Group 55fc7d6f-cc44-b4c0-e063-6294a90ae4fc 2026-07-06 Warnings Exact identifier unii: 362O9ITL9D
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.