FDA.reportPublic FDA data

Isoxsuprine Hydrochloride

Manufacturer
Darmerica, LLC
Effective date
2025-12-29
Label type
BULK INGREDIENT - ANIMAL DRUG
Version
4
Source
full-release
Hydrated at
2026-06-01 02:52:15

Label at a glance#

ProductIsoxsuprine Hydrochloride
Active ingredientISOXSUPRINE HYDROCHLORIDE
Label structure1 sections

Label contents#

Full prescribing information#

Isoxsuprine HCl

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Isoxsuprine HClIsoxsuprine HClIsoxsuprine HClIsoxsuprine HCl

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

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
71052-17271052-172-20, 71052-172-05, 71052-172-50, 71052-172-10, 71052-172-25, 71052-172-99

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
ISOXSUPRINE HYDROCHLORIDEV74TEQ36COACTIR

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

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