NDC 55529-161-42 - Midamox for Cats

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
55529-161
Requested NDC
55529-161-42
Package NDCs from labels
55529-161-40, 55529-161-42, 55529-161-45
Manufacturer
Norbrook Laboratories Limited | Norbrook Manufacturing Ltd
Effective date
2023-12-19
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Midamox for Cats - Norbrook Laboratories Limited | Norbrook Manufacturing LtdNorbrook Laboratories Limited | Norbrook Manufacturing Ltd2023-12-19PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55529-161-40Midamox for Cats0.23 mL in 1 APPLICATORSOLUTION0.233
55529-161-40Midamox for Cats3 in 1 CARTONSOLUTION33
55529-161-42Midamox for Cats0.4 mL in 1 APPLICATORSOLUTION0.43
55529-161-42Midamox for Cats6 in 1 CARTONSOLUTION63
55529-161-45Midamox for Cats0.8 mL in 1 APPLICATORSOLUTION0.83
55529-161-45Midamox for Cats6 in 1 CARTONSOLUTION63

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55529-161MIDAMOX FOR CATS (IMIDACLOPRID AND MOXIDECTIN) SOLUTION [NORBROOK LABORATORIES LIMITED]36 package rows20231220_4e3e11f4-e667-46bf-84cc-1a5dafd45a5a.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.