FDA.reportPublic FDA data

Protirelin Acetate

Manufacturer
Suzhou Qianyuan Biotechnology Co., Ltd.
Effective date
2022-11-30
Label type
BULK INGREDIENT - ANIMAL DRUG
Version
1
Source
full-release
Hydrated at
2026-06-01 02:50:36

Label at a glance#

ProductProtirelin Acetate
Active ingredientPROTIRELIN
Label structure1 sections

Label contents#

Full prescribing information#

Protirelin Acetate

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage descriptionimage descriptionimage description

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82773-003-01Protirelin Acetate10 g in 1 JARPOWDER101
82773-003-02Protirelin Acetate1 g in 1 VIALPOWDER11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82773-003PROTIRELIN ACETATE POWDER [SUZHOU QIANYUAN BIOTECHNOLOGY CO., LTD.]12 package rows20221202_fc1ace77-7dcb-4d98-bf69-a59073425923.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
82773-00382773-003-02, 82773-003-01

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.