Moxidectin

Manufacturer: Livzon New North River Pharmaceutical Co., Ltd.
Effective date: 2026-09-23
Label type: BULK INGREDIENT - ANIMAL DRUG
Version: 13
Source: daily-update
Hydrated at: 2026-09-26 01:01:56

Label at a glance#

ProductMoxidectin

Active ingredientMOXIDECTIN

Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Moxidectin label

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
ece42924-1f10-42a5-af85-87a1c603c9c4	Product name	1	20180807

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version	Uploaded
MOXIDECTIN	ACTIVE INGREDIENT	NGU5H31YO9	1
MOXIDECTIN	ACTIVE MOIETY	NGU5H31YO9	1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 1 matching rows.

Moxidectin

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
20076-1235	20076-1235-2, 20076-1235-3

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 1 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
MOXIDECTIN	NGU5H31YO9	ACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
Version	Effective date	Source	Hydrated
12	2024-12-24	full-release	2026-06-01 02:51:21

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	Name fallback brand name: Moxidectin generic name: MOXIDECTIN

Reported adverse events (FAERS/openFDA)#

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