Home NDC 49452-3035-6 NDC 49452-3035-6 - Fenbendazole 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 49452-3035
Requested NDC 49452-3035-6
Package NDCs from labels 49452-3035-1, 49452-3035-2, 49452-3035-3, 49452-3035-4, 49452-3035-5, 49452-3035-6
Manufacturer Spectrum Laboratory Products, Inc.
Effective date 2021-01-26
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Fenbendazole, USP Spectrum Laboratory Products, Inc. 2021-01-26 BULK INGREDIENT
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 49452-3035-1 Fenbendazole 5 g in 1 BOTTLE, GLASS POWDER 5 4 49452-3035-2 Fenbendazole 25 g in 1 BOTTLE, GLASS POWDER 25 4 49452-3035-3 Fenbendazole 100 g in 1 BOTTLE, GLASS POWDER 100 4 49452-3035-4 Fenbendazole 1000 g in 1 BOTTLE, GLASS POWDER 1000 4 49452-3035-5 Fenbendazole 25000 g in 1 DRUM POWDER 25000 4 49452-3035-6 Fenbendazole 5000 g in 1 PAIL POWDER 5000 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 49452-3035 FENBENDAZOLE POWDER [SPECTRUM LABORATORY PRODUCTS, INC.] 4 6 package rows 20210128_c4f6cd48-d024-42d1-9932-c5b64be41dd7.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 ยท 1 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.