FDA.reportPublic FDA data

Histrelin Acetate

Manufacturer
Zhejiang Peptites Biotech Co., Ltd
Effective date
2022-12-29
Label type
BULK INGREDIENT - ANIMAL DRUG
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:41:57

Label at a glance#

ProductHistrelin Acetate
Active ingredientHISTRELIN ACETATE
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

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
73569-03773569-037-01

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
HISTRELIN ACETATEQMG7HLD1ZEACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
SUPPRELIN LAHISTRELIN ACETATEEndo USA, Inc.d8fb000e-3cc9-4803-b71d-2cc5976619772025-09-25Warnings, Adverse reactionsName fallback
generic name: HISTRELIN ACETATE

Reported adverse events (FAERS/openFDA)#

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