FDA.reportPublic FDA data

NDC 73309-161-01 - Oxytetracycline Hydrochloride

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
73309-161
Requested NDC
73309-161-01
Package NDCs from labels
73309-161-01
Manufacturer
BLUEBAY SHANDONG CO.,LTD
Effective date
2021-04-12
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Oxytetracycline Hydrochloride - BLUEBAY SHANDONG CO.,LTDBLUEBAY SHANDONG CO.,LTD2021-04-12BULK INGREDIENT

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73309-161-01Oxytetracycline Hydrochloride1 kg in 1 BAGPOWDER12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73309-161OXYTETRACYCLINE HYDROCHLORIDE POWDER [BLUEBAY SHANDONG CO.,LTD]21 package rows20210413_bc186254-c539-445b-a253-59fbc8cd9074.zip

Reported adverse events (FAERS/openFDA)#

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