Home NDC 61133-5600 NDC 61133-5600 - BiloVet 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 61133-5600
Package NDCs from labels 61133-5600-2, 61133-5600-1
Manufacturer Bimeda, Inc.
Effective date 2024-09-18
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type BiloVet - Bimeda, Inc. Bimeda, Inc. 2024-09-18 PRESCRIPTION ANIMAL DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 61133-5600-1 BiloVet 100 g in 1 JAR POWDER, FOR SOLUTION 100 23 61133-5600-2 BiloVet 100 g in 1 PACKET POWDER, FOR SOLUTION 100 23
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 61133-5600 BILOVET (TYLOSIN TARTRATE) POWDER, FOR SOLUTION [BIMEDA, INC.] 23 2 package rows 20240920_a7335bfe-db82-4ff5-8072-1844110f752d.zip
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.