NDC 72341-011 - Sunburst Orange Barb

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: 72341-011
Package NDCs from labels: 72341-011-01
Manufacturer: GloFish LLC
Effective date: 2026-06-10
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 Barb - GloFish LLC	GloFish LLC	2026-06-10	Intentional Animal Genomic Alteration Label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
72341-011-01	Sunburst Orange Barb	1 [Amb'a'1'U] in 1 NOT APPLICABLE	NOT APPLICABLE	1		5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72341-011	SUNBURST ORANGE BARB (SUNBURST ORANGE BARB TRANSGENIC WHOLE (OB2019 RDNA CONSTRUCT)) NOT APPLICABLE [GLOFISH LLC]	5	1 package rows	20230519_5100b921-aff3-47f1-9448-71b3d83f2edc.zip

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.