FDA.reportPublic FDA data

Oxaceprol

Manufacturer
BLUEBAY SHANDONG CO.,LTD
Effective date
2021-12-31
Label type
BULK INGREDIENT
Version
4
Source
full-release
Hydrated at
2026-06-01 02:50:18

Label at a glance#

ProductOxaceprol
Active ingredientOxaceprol
Label structure1 sections

Label contents#

Full prescribing information#

Oxaceprol

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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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

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
73309-07973309-079-01, 73309-079-02, 73309-079-03, 73309-079-04

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
OxaceprolQ0XV76B96LACTIB

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

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