NDC 42662-001 - Orbifloxacin

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
42662-001
Package NDCs from labels
42662-001-01
Manufacturer
KATAYAMA SEIYAKUSYO CO., LTD. | KATAYAMA SEIYAKUSHO CO.,LTD.
Effective date
2022-12-19
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Orbifloxacin - KATAYAMA SEIYAKUSYO CO., LTD. | KATAYAMA SEIYAKUSHO CO.,LTD.KATAYAMA SEIYAKUSYO CO., LTD. | KATAYAMA SEIYAKUSHO CO.,LTD.2022-12-19BULK INGREDIENT - ANIMAL DRUG

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
42662-001-01Orbifloxacin30 kg in 1 DRUMPOWDER304

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
42662-001ORBIFLOXACIN POWDER [KATAYAMA SEIYAKUSYO CO., LTD.]41 package rows20221221_7d413fa4-2c5d-44df-b151-833d0a43578a.zip