FDA.reportPublic FDA data

NDC 71052-089-05 - Deslorelin 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
71052-089
Requested NDC
71052-089-05
Package NDCs from labels
71052-089-01, 71052-089-05
Manufacturer
Darmerica LLC
Effective date
2026-10-07
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Deslorelin Acetate - Darmerica LLCDarmerica LLC2026-10-07BULK INGREDIENT - ANIMAL DRUG

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71052-089-01Deslorelin Acetate1 g in 1 PACKAGEPOWDER14
71052-089-05Deslorelin Acetate5 g in 1 PACKAGEPOWDER54

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71052-089DESLORELIN ACETATE POWDER [DARMERICA LLC]32 package rows20250427_802eae17-616f-4f54-b118-c38e8711135a.zip

Reported adverse events (FAERS/openFDA)#

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