FDA.reportPublic FDA data

PROTIRELIN

Manufacturer
MAEDA INC
Effective date
2026-03-23
Label type
BULK INGREDIENT - ANIMAL DRUG
Version
1
Source
full-release
Hydrated at
2026-06-01 02:52:42

Label at a glance#

ProductPROTIRELIN
Active ingredientPROTIRELIN
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

protirelinlabelfile.jpgPACKAGE LABEL IMAGEPACKAGE LABEL IMAGE

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
86184-318-01PROTIRELIN1 g in 1 PACKAGEPOWDER11

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
86184-31886184-318-01

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
PROTIRELIN5Y5F15120WACTIB

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

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