Home DailyMed 7d413fa4-2c5d-44df-b151-833d0a43578a Orbifloxacin Drug label information. FDA.report displays public Structured Product Labeling data from DailyMed and legacy FDA.report DailyMed cache rows. This page is not medical advice, prescribing advice, or a substitute for the official label reviewed by a qualified healthcare professional. Labeling can change; when a current hydrated DailyMed SPL record is available, FDA.report shows that newer record before legacy cached files.
Manufacturer KATAYAMA SEIYAKUSYO CO., LTD. | KATAYAMA SEIYAKUSHO CO.,LTD.
Effective date 2022-12-19
Label type BULK INGREDIENT - ANIMAL DRUG
Version 4
Source full-release
Hydrated at 2026-06-01 02:50:37 Label at a glance# Product Orbifloxacin
Active ingredient Orbifloxacin
Label structure 1 sections
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 42662-001-01 Orbifloxacin 30 kg in 1 DRUM POWDER 30 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 42662-001 ORBIFLOXACIN POWDER [KATAYAMA SEIYAKUSYO CO., LTD.] 4 1 package rows 20221221_7d413fa4-2c5d-44df-b151-833d0a43578a.zip
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Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.