NDC 73309-331 - Luliconazole

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: 73309-331
Package NDCs from labels: 73309-331-01
Manufacturer: BLUEBAY SHANDONG CO.,LTD
Effective date: 2021-09-13
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Luliconazole - BLUEBAY SHANDONG CO.,LTD	BLUEBAY SHANDONG CO.,LTD	2021-09-13	BULK INGREDIENT

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
73309-331-01	Luliconazole	100 g in 1 JAR	POWDER	100		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
73309-331	LULICONAZOLE POWDER [BLUEBAY SHANDONG CO.,LTD]	1	1 package rows	20210915_5ed04460-1369-4985-8ebd-23f8f6ad6946.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 2 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
LULICONAZOLE	LULICONAZOLE	Oceanside Pharmaceuticals	7ccda3ba-9c98-468d-83c6-7f0cc7c88c33	2020-04-30	Adverse reactions	Exact identifier unii: RE91AN4S8G
Luzu	LULICONAZOLE	Bausch Health US, LLC	a7016010-ce43-4c09-8d21-aeb697ffed31	2020-04-01	Adverse reactions	Exact identifier unii: RE91AN4S8G

Reported adverse events (FAERS/openFDA)#

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