FDA.reportPublic FDA data

NDC 0026-9711 - Viadur

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
0026-9711
Package NDCs from labels
0026-9711-01
Manufacturer
Bayer Pharmaceuticals Corporation
Effective date
2006-05-10
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Viadur - Bayer Pharmaceuticals CorporationBayer Pharmaceuticals Corporation2006-05-10HUMAN PRESCRIPTION DRUG LABELING

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0026-9711-01Viadur1 in 1 BOXKIT11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0026-9711VIADUR (LEUPROLIDE ACETATE) [BAYER PHARMACEUTICALS CORPORATION]11 package rows20071010_82c5998f-2253-4880-9be5-feaba553d5d1.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
LEUPROLIDE ACETATEACTIVE INGREDIENT37JNS02E7VVIADUR (LEUPROLIDE ACETATE) [BAYER PHARMACEUTICALS CORPORATION]1
Lidocaine hydrochlorideACTIVE INGREDIENTV13007Z41AVIADUR (LEUPROLIDE ACETATE) [BAYER PHARMACEUTICALS CORPORATION]1
LEUPROLIDEACTIVE MOIETYEFY6W0M8TGVIADUR (LEUPROLIDE ACETATE) [BAYER PHARMACEUTICALS CORPORATION]1
lidocaineACTIVE MOIETY98PI200987VIADUR (LEUPROLIDE ACETATE) [BAYER PHARMACEUTICALS CORPORATION]1
Dimethyl SulfoxideINACTIVE INGREDIENTYOW8V9698HVIADUR (LEUPROLIDE ACETATE) [BAYER PHARMACEUTICALS CORPORATION]1
magnesium stearateINACTIVE INGREDIENT70097M6I30VIADUR (LEUPROLIDE ACETATE) [BAYER PHARMACEUTICALS CORPORATION]1
Polyethylene glycolINACTIVE INGREDIENTVIADUR (LEUPROLIDE ACETATE) [BAYER PHARMACEUTICALS CORPORATION]1
PovidoneINACTIVE INGREDIENTVIADUR (LEUPROLIDE ACETATE) [BAYER PHARMACEUTICALS CORPORATION]1
SiliconeINACTIVE INGREDIENTVIADUR (LEUPROLIDE ACETATE) [BAYER PHARMACEUTICALS CORPORATION]1
Sodium Carboxymethyl CelluloseINACTIVE INGREDIENTVIADUR (LEUPROLIDE ACETATE) [BAYER PHARMACEUTICALS CORPORATION]1
sodium chlorideINACTIVE INGREDIENT451W47IQ8XVIADUR (LEUPROLIDE ACETATE) [BAYER PHARMACEUTICALS CORPORATION]1
waterINACTIVE INGREDIENT059QF0KO0RVIADUR (LEUPROLIDE ACETATE) [BAYER PHARMACEUTICALS CORPORATION]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 1 of 2 · 31 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Lidocaine HydrochlorideLIDOCAINE HYDROCHLORIDEHospira, Inc.3b2dd84e-cee8-4e58-d494-395a65a353a02026-08-05Warnings, Adverse reactionsExact identifier
rxcui: 1010671
Lidocaine hydrochlorideLIDOCAINE HYDROCHLORIDEMedical Purchasing Solutions, LLC573a7298-b02e-230c-e063-6294a90a269c2026-07-22Warnings, Adverse reactionsExact identifier
rxcui: 1010671
Lidocaine hydrochlorideLIDOCAINE HYDROCHLORIDECamber Pharmaceuticals, Inc.9a1418e2-b208-4e5c-b5f8-21b3a691a5782026-04-13Warnings, Adverse reactionsExact identifier
rxcui: 1010671
Lidocaine HydrochlorideLIDOCAINE HYDROCHLORIDEAnthea Pharma Private Limited240c4744-e58c-4c08-93ad-8d6418c4f8a92026-02-11Warnings, Adverse reactionsExact identifier
rxcui: 1010671
Lidocaine HydrochlorideLIDOCAINE HYDROCHLORIDESportpharm LLC415a29c1-101a-4ac2-9ba9-b419a1ce56002026-02-03Warnings, Adverse reactionsExact identifier
rxcui: 1010671
XylocaineLIDOCAINE HYDROCHLORIDESportpharm LLC94155012-b1fc-430a-a1f5-30c21f4a3f802026-02-03Warnings, Adverse reactionsExact identifier
rxcui: 1010671
Lidocaine HydrochlorideLIDOCAINE HYDROCHLORIDEProPharma Distribution42d9e4cf-ca73-ec6d-e063-6394a90ae9372025-12-18Warnings, Adverse reactionsExact identifier
rxcui: 1010671
Lidocaine HydrochlorideLIDOCAINE HYDROCHLORIDEBrookfield Pharmaceuticals, LLC.e824ba5b-3289-5ad4-e053-2995a90acc202025-11-27Warnings, Adverse reactionsExact identifier
rxcui: 1010671
XylocaineLIDOCAINE HCLHenry Schein, Inc.a6019956-a6e0-4988-a870-6aee06c354c32025-11-07Warnings, Adverse reactionsExact identifier
rxcui: 1010671
LidocaineLIDOCAINE HYDROCHLORIDEA-S Medication Solutionse6c83ad7-2821-432b-8610-0f54cfe610cb2025-10-21Warnings, Adverse reactionsExact identifier
rxcui: 1010671
Lidocaine HydrochlorideLIDOCAINE HYDROCHLORIDE ANHYDROUSHenry Schein, Inc.bb53bb10-bb36-4c9b-b632-71455615f9f32025-09-29Warnings, Adverse reactionsExact identifier
rxcui: 1010671
LIDOCAINE HCILIDOCAINE HCIHF Acquisition Co LLC, DBA HealthFirst953471e2-9efb-adf0-e053-2a95a90afd952025-07-09Warnings, Adverse reactionsExact identifier
rxcui: 1010671
LIDOCAINE HYDROCHLORIDELIDOCAINE HYDROCHLORIDEHenry Schein, Inc.767374af-89d1-4c19-bd8e-480699b45cf72025-06-11Warnings, Adverse reactionsExact identifier
rxcui: 1010671
XylocaineLIDOCAINE HYDROCHLORIDEAsclemed USA, Inc.25370b0f-0ac6-4a03-abe6-d73d651921802025-05-31Warnings, Adverse reactionsExact identifier
rxcui: 1010671
Lidocaine HydrochlorideLIDOCAINE HYDROCHLORIDEHuons Co., Ltd.8ec2d256-fc4f-44f6-bee2-eef2bf3bf5802025-05-09Warnings, Adverse reactionsExact identifier
rxcui: 1010671
LidocaineLIDOCAINE HYDROCHLORIDEHikma Pharmaceuticals USA Inc.5523fdfe-69fd-49a5-b51f-73e2223d49a92025-05-01Warnings, Adverse reactionsExact identifier
rxcui: 1010671
XylocaineLIDOCAINE HYDROCHLORIDE,EPINEPHRINE BITARTRATEFresenius Kabi USA, LLC4dd52202-8eef-4136-92dd-ada573b7cf742025-04-22Warnings, Adverse reactionsExact identifier
rxcui: 1010671
Lidocaine hydrochlorideLIDOCAINE HYDROCHLORIDENorthStar RxLLC6a7fa6c5-b550-46ac-99a3-5c49339e6dbd2025-02-19Warnings, Adverse reactionsExact identifier
rxcui: 1010671
Lidocaine HydrochlorideLIDOCAINE HYDROCHLORIDEEugia US LLCccc38d8a-43fd-44c0-985e-32af9ed956ab2025-02-03Warnings, Adverse reactionsExact identifier
rxcui: 1010671
1% LIDOCAINE HCI1% LIDOCAINE HCIHF Acquisition Co LLC, DBA HealthFirst999b1c7b-3495-926a-e053-2a95a90ab2062025-01-08Warnings, Adverse reactionsExact identifier
rxcui: 1010671

Reported adverse events (FAERS/openFDA)#

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