Home NDC 69866-2000 NDC 69866-2000 - NEXOBRID 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 69866-2000
Package NDCs from labels 69866-2000-1
Manufacturer Vericel Corporation
Effective date 2025-09-11
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type NEXOBRID - Vericel Corporation Vericel Corporation 2025-09-11 HUMAN PRESCRIPTION DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 69866-2000-1 NEXOBRID 2 g in 1 VIAL, GLASS POWDER 2 g 158 mg in 1g 10
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69866-2000 NEXOBRID (ANACAULASE-BCDB) KIT [VERICEL CORPORATION] 9 Unmatched 20250212_1a2f23ad-78ef-43fa-9864-6bd77aac9e57.zip