FDA.reportPublic FDA data

NDC 71052-172-99 - Isoxsuprine Hydrochloride

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
71052-172
Requested NDC
71052-172-99
Package NDCs from labels
71052-172-20, 71052-172-05, 71052-172-50, 71052-172-10, 71052-172-25, 71052-172-99
Manufacturer
Darmerica, LLC
Effective date
2025-12-29
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Isoxsuprine Hydrochloride - Darmerica, LLCDarmerica, LLC2025-12-29BULK INGREDIENT - ANIMAL DRUG

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71052-172-05Isoxsuprine Hydrochloride5 kg in 1 PACKAGEPOWDER54
71052-172-10Isoxsuprine Hydrochloride0.1 kg in 1 PACKAGEPOWDER0.14
71052-172-20Isoxsuprine Hydrochloride1 kg in 1 PACKAGEPOWDER14
71052-172-25Isoxsuprine Hydrochloride0.25 kg in 1 PACKAGEPOWDER0.254
71052-172-50Isoxsuprine Hydrochloride0.5 kg in 1 PACKAGEPOWDER0.54
71052-172-99Isoxsuprine Hydrochloride25 kg in 1 PACKAGEPOWDER254

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71052-172ISOXSUPRINE HYDROCHLORIDE POWDER [DARMERICA, LLC]36 package rows20241222_8379953b-d951-42d6-951d-eaea944ce65d.zip

Reported adverse events (FAERS/openFDA)#

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