FDA.reportPublic FDA data

NDC 55529-192-05 - Tauramox

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
55529-192
Requested NDC
55529-192-05
Package NDCs from labels
55529-192-04, 55529-192-05
Manufacturer
Norbrook Laboratories Limited
Effective date
2023-05-01
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Tauramox - Norbrook Laboratories LimitedNorbrook Laboratories Limited2023-05-01OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55529-192-04Tauramox1 in 1 CARTONINJECTION, SOLUTION13
55529-192-04Tauramox250 mL in 1 VIAL, GLASSINJECTION, SOLUTION2503
55529-192-05Tauramox500 mL in 1 VIAL, GLASSINJECTION, SOLUTION5003
55529-192-05Tauramox1 in 1 CARTONINJECTION, SOLUTION13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55529-192TAURAMOX (MOXIDECTIN) INJECTION, SOLUTION [NORBROOK LABORATORIES LIMITED]34 package rows20241010_36feb63e-c146-45ea-b814-45022ae66d15.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 1 of 1 ยท 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
MoxidectinMOXIDECTINMedicines Development for Global Health6eb02ae9-9065-176f-e053-2991aa0ac8912026-07-30Warnings, Adverse reactionsExact identifier
unii: NGU5H31YO9

Reported adverse events (FAERS/openFDA)#

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