FDA.reportPublic FDA data

NDC 73309-220 - Betadex Sulfobutyl Ether Sodium

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
73309-220
Package NDCs from labels
73309-220-01, 73309-220-02
Manufacturer
BLUEBAY SHANDONG CO.,LTD
Effective date
2021-01-27
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Betadex Sulfobutyl Ether Sodium - BLUEBAY SHANDONG CO.,LTDBLUEBAY SHANDONG CO.,LTD2021-01-27BULK INGREDIENT

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73309-220-01Betadex Sulfobutyl Ether Sodium1 kg in 1 JARPOWDER12
73309-220-02Betadex Sulfobutyl Ether Sodium0.5 kg in 1 JARPOWDER0.52

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73309-220BETADEX SULFOBUTYL ETHER SODIUM POWDER [BLUEBAY SHANDONG CO.,LTD]22 package rows20210128_8dfd3efd-7f38-42ae-908c-7709186132b0.zip

Reported adverse events (FAERS/openFDA)#

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