FDA.reportPublic FDA data

Lufenuron

Manufacturer
AX Pharmaceutical Corp
Effective date
2024-11-28
Label type
BULK INGREDIENT - ANIMAL DRUG
Version
3
Source
full-release
Hydrated at
2026-06-01 02:51:17

Label at a glance#

ProductLufenuron
Active ingredientLUFENURON
Label structure1 sections

Label contents#

Full prescribing information#

Lufenuron

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73377-136-01Lufenuron5 kg in 1 DRUMPOWDER53
73377-136-02Lufenuron1 kg in 1 JARPOWDER13
73377-136-03Lufenuron0.5 kg in 1 JARPOWDER0.53

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73377-136LUFENURON POWDER [AX PHARMACEUTICAL CORP]33 package rows20241129_e203c33c-88cb-4a62-9a2a-bbdfb42cd2c1.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73377-13673377-136-01, 73377-136-02, 73377-136-03

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
NameUNIIKind
LUFENURON1R754M4918ACTIB

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

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