Home NDC 63732-2048-5 NDC 63732-2048-5 - Levamisole Hydrochloride 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 63732-2048
Requested NDC 63732-2048-5
Package NDCs from labels 63732-2048-4, 63732-2048-5
Manufacturer H3 Medical Inc.
Effective date 2019-09-04
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Levamisole Hydrochloride H3 Medical Inc. 2019-09-04 BULK INGREDIENT
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63732-2048-4 Levamisole Hydrochloride 100 g in 1 BOTTLE POWDER 100 1 63732-2048-5 Levamisole Hydrochloride 500 g in 1 BOTTLE POWDER 500 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 63732-2048 LEVAMISOLE HYDROCHLORIDE POWDER [H3 MEDICAL INC.] 1 2 package rows 20190905_22a903c0-c30f-4df6-8082-1bc23b68a8c2.zip
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.