FDA.reportPublic FDA data

NDC 73377-171 - Sulfadimethoxine

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
73377-171
Package NDCs from labels
73377-171-01
Manufacturer
AX Pharmaceutical Corp
Effective date
2026-01-19
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Sulfadimethoxine - AX Pharmaceutical CorpAX Pharmaceutical Corp2026-01-19BULK INGREDIENT - ANIMAL DRUG

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73377-171-01Sulfadimethoxine500 g in 1 JARPOWDER5002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73377-171SULFADIMETHOXINE POWDER [AX PHARMACEUTICAL CORP]11 package rows20220903_a9c395c4-a711-4fba-8d96-9f76cde78b41.zip

Reported adverse events (FAERS/openFDA)#

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