Home NDC 11789-042 NDC 11789-042 - ToxiBan 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 11789-042
Package NDCs from labels 11789-042-30, 11789-042-20
Manufacturer LLOYD, Inc. of Iowa
Effective date 2023-07-11
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type ToxiBan - LLOYD, Inc. of Iowa LLOYD, Inc. of Iowa 2023-07-11 OTC ANIMAL DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 11789-042-20 ToxiBan 5000 g in 1 PAIL GRANULE 5000 1 11789-042-30 ToxiBan 453.6 g in 1 BOTTLE GRANULE 453.6 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 11789-042 TOXIBAN (ACTIVATED CHARCOAL) GRANULE [LLOYD, INC. OF IOWA] 1 2 package rows 20230719_3b93af3c-b1ca-482d-beb9-973f5644b898.zip