NDC 73309-041 - Trametinib

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: 73309-041
Package NDCs from labels: 73309-041-01
Manufacturer: Bluebay Shandong Co, LTD. | Nanjing Chemlin Biomedical Science & Technology Co, Ltd.
Effective date: 2019-10-16
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Trametinib	Bluebay Shandong Co, LTD. \| Nanjing Chemlin Biomedical Science & Technology Co, Ltd.	2019-10-16	BULK INGREDIENT

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
73309-041-01	Trametinib	10 g in 1 JAR	POWDER	10		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
73309-041	TRAMETINIB POWDER [BLUEBAY SHANDONG CO, LTD.]	1	1 package rows	20191017_f5d46fbf-92d7-4d86-949c-97e52b07267b.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 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Mekinist	TRAMETINIB	Novartis Pharmaceuticals Corporation	0002ad27-779d-42ab-83b5-bc65453412a1	2026-05-07	Warnings, Adverse reactions	Name fallback generic name: TRAMETINIB

Reported adverse events (FAERS/openFDA)#

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