Home NDC 63833-627 NDC 63833-627 - Humate-P 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 63833-627
Package NDCs from labels 63833-627-01
Manufacturer CSL Behring GmbH
Effective date 2020-08-17
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Humate-P - CSL Behring GmbH CSL Behring GmbH 2020-08-17 PLASMA DERIVATIVE
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 63833-627-01 Humate-P 15 mL in 1 VIAL INJECTION, POWDER, LYOPHILIZED, 15 mL 80 [iU] in 1mL 16
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 63833-627 HUMATE-P (ANTIHEMOPHILIC FACTOR/VON WILLEBRAND FACTOR COMPLEX (HUMAN)) KIT [CSL BEHRING GMBH] 16 Unmatched 20200826_c5f4b63b-8d8b-45b3-b530-2f1c32a1b852.zip
DailyMed Socrata Ingredients#