NDC 52133-0047 - FEBANTEL

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
52133-0047
Package NDCs from labels
52133-0047-0
Manufacturer
F.I.S. Fabbrica Italiana Sintetici S.P.A.
Effective date
2024-11-22
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
FebantelF.I.S. Fabbrica Italiana Sintetici S.P.A.2024-11-22BULK INGREDIENT - ANIMAL DRUG

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52133-0047-0FEBANTEL50 kg in 1 DRUMPOWDER504

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
52133-0047FEBANTEL POWDER [F.I.S. FABBRICA ITALIANA SINTETICI S.P.A.]41 package rows20241127_ce164a56-ddfb-6098-e053-2a95a90add22.zip