FDA.reportPublic FDA data

NDC 73309-152 - romifidine hcl

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
73309-152
Package NDCs from labels
73309-152-01, 73309-152-02, 73309-152-03
Manufacturer
BLUEBAY SHANDONG CO.,LTD
Effective date
2020-12-02
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
romifidine hcl - BLUEBAY SHANDONG CO.,LTDBLUEBAY SHANDONG CO.,LTD2020-12-02BULK INGREDIENT

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73309-152-01romifidine hcl10 g in 1 JARPOWDER103
73309-152-02romifidine hcl5 g in 1 JARPOWDER53
73309-152-03romifidine hcl100 g in 1 JARPOWDER1003

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73309-152ROMIFIDINE HCL POWDER [BLUEBAY SHANDONG CO.,LTD]33 package rows20201203_502ad59c-ff0d-42f0-97de-d22a9b907eea.zip

Reported adverse events (FAERS/openFDA)#

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