FDA.reportPublic FDA data

NDC 73377-089 - Marbofloxacin

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
73377-089
Package NDCs from labels
73377-089-01, 73377-089-02, 73377-089-03
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
Marbofloxacin - AX Pharmaceutical CorpAX Pharmaceutical Corp2026-01-19BULK INGREDIENT - ANIMAL DRUG

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73377-089-01Marbofloxacin250 g in 1 JARPOWDER2505
73377-089-02Marbofloxacin100 g in 1 JARPOWDER1005
73377-089-03Marbofloxacin1000 g in 1 JARPOWDER10005

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73377-089MARBOFLOXACIN POWDER [AX PHARMACEUTICAL CORP]43 package rows20231110_b0e6d6a4-3dae-48b6-a4cd-539570068aee.zip

Reported adverse events (FAERS/openFDA)#

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