FDA.reportPublic FDA data

NDC 73377-136 - Lufenuron

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
73377-136
Package NDCs from labels
73377-136-01, 73377-136-02, 73377-136-03
Manufacturer
AX Pharmaceutical Corp
Effective date
2024-11-28
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Lufenuron - AX Pharmaceutical CorpAX Pharmaceutical Corp2024-11-28BULK INGREDIENT - ANIMAL DRUG

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

Reported adverse events (FAERS/openFDA)#

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