Home NDC 63833-835 NDC 63833-835 - Berinert 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 63833-835
Package NDCs from labels 63833-835-01
Manufacturer CSL Behring GmbH
Effective date 2021-09-21
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Berinert - CSL Behring GmbH CSL Behring GmbH 2021-09-21 PLASMA DERIVATIVE
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63833-835-01 Berinert 10 mL in 1 VIAL INJECTION, POWDER, LYOPHILIZED, 10 mL 500 [iU] in 10mL 33
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 63833-835 BERINERT (HUMAN C1-ESTERASE INHIBITOR) KIT [CSL BEHRING GMBH] 33 Unmatched 20210928_8ea0c7fe-da9d-4218-a080-0509e09bedc6.zip
DailyMed Socrata Ingredients#