Home NDC 72341-009 NDC 72341-009 - Sunburst Orange Danio 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 72341-009
Package NDCs from labels 72341-009-01
Manufacturer GloFish LLC
Effective date 2026-04-28
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Sunburst Orange Danio - GloFish LLC GloFish LLC 2026-04-28 INTENTIONAL ANIMAL GENOMIC ALTERATION LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 72341-009-01 Sunburst Orange Danio 1 [Amb'a'1'U] in 1 NOT APPLICABLE NOT APPLICABLE 1 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72341-009 SUNBURST ORANGE DANIO (SUNBURST ORANGE DANIO TRANSGENIC WHOLE (YZF2010 RDNA CONSTRUCT)) NOT APPLICABLE [GLOFISH LLC] 3 1 package rows 20230523_172f01c1-96aa-43a1-a864-1b655b11f610.zip