FDA.reportPublic FDA data

NDC 73309-079 - Oxaceprol

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
73309-079
Package NDCs from labels
73309-079-01, 73309-079-02, 73309-079-03, 73309-079-04
Manufacturer
BLUEBAY SHANDONG CO.,LTD
Effective date
2021-12-31
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Oxaceprol - BLUEBAY SHANDONG CO.,LTDBLUEBAY SHANDONG CO.,LTD2021-12-31BULK INGREDIENT

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73309-079-01Oxaceprol500 g in 1 JARPOWDER5004
73309-079-02Oxaceprol5000 g in 1 DRUMPOWDER50004
73309-079-03Oxaceprol1000 g in 1 DRUMPOWDER10004
73309-079-04Oxaceprol100 g in 1 JARPOWDER1004

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73309-079OXACEPROL POWDER [BLUEBAY SHANDONG CO.,LTD]44 package rows20220106_8a33ecf1-0c9a-4f36-b2be-dd262c8fa716.zip

Reported adverse events (FAERS/openFDA)#

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