NDC 86136-116-31 - 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: 86136-116
Requested NDC: 86136-116-31
Package NDCs from labels: 86136-116-31
Manufacturer: MWI/VetOne | Bimeda, Inc. | Bimeda-MTC Animal Health
Effective date: 2024-10-08
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
MoxiSolv - MWI/VetOne \| Bimeda, Inc. \| Bimeda-MTC Animal Health	MWI/VetOne \| Bimeda, Inc. \| Bimeda-MTC Animal Health	2024-10-08	OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
86136-116-31	MoxiSolv	500 mL in 1 BOTTLE	INJECTION, SOLUTION	500		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
86136-116	MOXISOLV (MOXIDECTIN) INJECTION, SOLUTION [MWI/VETONE]	1	1 package rows	20241010_15403e7f-e129-4e16-8805-2066c11489e5.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 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Moxidectin	MOXIDECTIN	Medicines Development for Global Health	6eb02ae9-9065-176f-e053-2991aa0ac891	2026-07-30	Warnings, Adverse reactions	Exact identifier unii: NGU5H31YO9

Reported adverse events (FAERS/openFDA)#

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