NDC 73309-008-01 - Imatinib Mesylate

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
73309-008
Requested NDC
73309-008-01
Package NDCs from labels
73309-008-01, 73309-008-02, 73309-008-03, 73309-008-04
Manufacturer
BLUEBAY SHANDONG CO.,LTD
Effective date
2020-12-02
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Imatinib Mesylate - BLUEBAY SHANDONG CO.,LTDBLUEBAY SHANDONG CO.,LTD2020-12-02BULK INGREDIENT

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73309-008-01Imatinib Mesylate500 g in 1 JARPOWDER5003
73309-008-02Imatinib Mesylate1900 g in 1 JARPOWDER19003
73309-008-03Imatinib Mesylate1000 g in 1 JARPOWDER10003
73309-008-04Imatinib Mesylate900 g in 1 JARPOWDER9003

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73309-008IMATINIB MESYLATE POWDER [BLUEBAY SHANDONG CO.,LTD]34 package rows20201203_14b761ae-d40b-4907-ae66-5dfe75075cd6.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 2 of 2 · 22 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Imatinib mesylateIMATINIB MESYLATEArmas Pharmaceuticals Inc.2e931c49-6c9f-41e2-a34b-5f01cd295b562019-03-04Warnings, Adverse reactionsExact identifier
unii: 8A1O1M485B
Imatinib mesylateIMATINIB MESYLATEAscend Laboratories, LLC7579620e-3748-46fa-8295-f9b47d0aa5b82019-02-01Warnings, Adverse reactionsExact identifier
unii: 8A1O1M485B

Reported adverse events (FAERS/openFDA)#

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