FDA.reportPublic FDA data

NDC 73569-037 - Histrelin Acetate

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
73569-037
Package NDCs from labels
73569-037-01
Manufacturer
Zhejiang Peptites Biotech Co., Ltd
Effective date
2022-12-29
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Histrelin Acetate - Zhejiang Peptites Biotech Co., LtdZhejiang Peptites Biotech Co., Ltd2022-12-29BULK INGREDIENT - ANIMAL DRUG

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 ยท 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 reactionsExact identifier
unii: QMG7HLD1ZE

Reported adverse events (FAERS/openFDA)#

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