FDA.reportPublic FDA data

NDC 73309-102 - Propantheline Bromide

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
73309-102
Package NDCs from labels
73309-102-01, 73309-102-02, 73309-102-03
Manufacturer
BLUEBAY SHANDONG CO.,LTD
Effective date
2021-06-09
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Propantheline Bromide - BLUEBAY SHANDONG CO.,LTDBLUEBAY SHANDONG CO.,LTD2021-06-09BULK INGREDIENT

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73309-102-01Propantheline Bromide100 g in 1 JARPOWDER1003
73309-102-02Propantheline Bromide50 g in 1 JARPOWDER503
73309-102-03Propantheline Bromide25 g in 1 JARPOWDER253

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73309-102PROPANTHELINE BROMIDE POWDER [BLUEBAY SHANDONG CO.,LTD]33 package rows20210611_de0fb712-9635-4dd9-b602-b940ca54f0ef.zip

Reported adverse events (FAERS/openFDA)#

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