FDA.reportPublic FDA data

Propantheline Bromide

Manufacturer
BLUEBAY SHANDONG CO.,LTD
Effective date
2021-06-09
Label type
BULK INGREDIENT
Version
3
Source
full-release
Hydrated at
2026-06-01 02:50:01

Label at a glance#

ProductPropantheline Bromide
Active ingredientPROPANTHELINE BROMIDE
Label structure1 sections

Label contents#

Full prescribing information#

Propantheline Bromide

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

image descriptionimage description

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DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
9c98c371-d578-d114-4b77-748472617b70Product name120140508

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

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
73309-10273309-102-01, 73309-102-02, 73309-102-03

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
PROPANTHELINE BROMIDEUX9Z118X9FACTIB

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

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