FDA.reportPublic FDA data

Oxytetracycline Hydrochloride

Manufacturer
BLUEBAY SHANDONG CO.,LTD
Effective date
2021-04-12
Label type
BULK INGREDIENT
Version
2
Source
full-release
Hydrated at
2026-06-01 02:49:57

Label at a glance#

ProductOxytetracycline Hydrochloride
Active ingredientOXYTETRACYCLINE HYDROCHLORIDE
Label structure1 sections

Label contents#

Full prescribing information#

Oxytetracycline Hydrochloride

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

image descriptionimage description

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

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 1 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73309-16173309-161-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 1 matching rows.

Name, UNII, Kind table
NameUNIIKind
OXYTETRACYCLINE HYDROCHLORIDE4U7K4N52ZMACTIM

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

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