FDA.reportPublic FDA data

NDC 71052-551-25 - Butylscopolamine 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
71052-551
Requested NDC
71052-551-25
Package NDCs from labels
71052-551-25, 71052-551-05, 71052-551-50, 71052-551-10
Manufacturer
DARMERICA, LLC
Effective date
2026-08-21
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Butylscopolamine Bromide - DARMERICA, LLCDARMERICA, LLC2026-08-21BULK INGREDIENT - ANIMAL DRUG

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71052-551-05Butylscopolamine Bromide0.050 kg in 1 PACKAGEPOWDER0.0503
71052-551-25Butylscopolamine Bromide0.025 kg in 1 PACKAGEPOWDER0.0253
71052-551-50Butylscopolamine Bromide0.0050 kg in 1 PACKAGEPOWDER0.00503

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71052-551BUTYLSCOPOLAMINE BROMIDE POWDER [DARMERICA, LLC]23 package rows20240509_f9605d6f-e276-4c12-8a58-1a0c8e67f1c9.zip

Reported adverse events (FAERS/openFDA)#

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