FDA.reportPublic FDA data

n-Butylscopolammonium Bromide

Manufacturer
BLUEBAY SHANDONG CO.,LTD
Effective date
2019-09-12
Label type
BULK INGREDIENT
Version
1
Source
full-release
Hydrated at
2026-06-01 02:49:22

Label at a glance#

Productn-Butylscopolammonium Bromide
Active ingredientBUTYLSCOPOLAMINE BROMIDE
Label structure1 sections

Label contents#

Full prescribing information#

n-Butylscopolammonium Bromide

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73309-033-01n-Butylscopolammonium Bromide50 g in 1 JARPOWDER501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73309-033N-BUTYLSCOPOLAMMONIUM BROMIDE POWDER [BLUEBAY SHANDONG CO.,LTD]11 package rows20190913_c7f7f009-4e21-46c1-91b3-97969da7e1a3.zip

Products#

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

DailyMed product names page 1 of 1 · 2 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73309-03373309-033-01

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
BUTYLSCOPOLAMINE BROMIDE0GH9JX37C8ACTIM

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

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