NDC 61133-4013-2 - MoxiSolv

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
61133-4013
Requested NDC
61133-4013-2
Package NDCs from labels
61133-4013-2
Manufacturer
Bimeda, Inc. | Bimeda-MTC Animal Health
Effective date
2025-03-19
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
MoxiSolv - Bimeda, Inc. | Bimeda-MTC Animal HealthBimeda, Inc. | Bimeda-MTC Animal Health2025-03-19OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61133-4013-2MoxiSolv500 mL in 1 BOTTLEINJECTION, SOLUTION5003

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
61133-4013MOXISOLV (MOXIDECTIN) INJECTION, SOLUTION [BIMEDA, INC.]31 package rows20250322_8eefc52a-6f0f-486f-8a27-94e457a42a06.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.