NDC 73309-211 - Trametinib Dimethyl Sulfoxide

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: 73309-211
Package NDCs from labels: 73309-211-01, 73309-211-02, 73309-211-03
Manufacturer: BLUEBAY SHANDONG CO.,LTD
Effective date: 2021-10-22
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Trametinib Dimethyl Sulfoxide - BLUEBAY SHANDONG CO.,LTD	BLUEBAY SHANDONG CO.,LTD	2021-10-22	BULK INGREDIENT

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
73309-211-01	Trametinib Dimethyl Sulfoxide	1 g in 1 JAR	POWDER	1	2
73309-211-02	Trametinib Dimethyl Sulfoxide	5 g in 1 JAR	POWDER	5	2
73309-211-03	Trametinib Dimethyl Sulfoxide	10 g in 1 JAR	POWDER	10	2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
73309-211	TRAMETINIB DIMETHYL SULFOXIDE POWDER [BLUEBAY SHANDONG CO.,LTD]	2	3 package rows	20211027_49d5f5ef-0d09-4045-9cae-a791d4fe0bce.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	Exact identifier unii: BSB9VJ5TUT

Reported adverse events (FAERS/openFDA)#

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