FDA.reportPublic FDA data

APOMORPHINE HYDROCHLORIDE - Food and Drug Administration

Manufacturer
Food and Drug Administration
Effective date
2020-10-21
Label type
Indexing - product concept
Version
1
Source
full-release
Hydrated at
2026-06-05 00:19:19

Label at a glance#

ProductAPOMORPHINE HYDROCHLORIDE
Active ingredientAPOMORPHINE HYDROCHLORIDE

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 2 matching rows.

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
APOMORPHINE HYDROCHLORIDEF39049Y068ACTIB
APOMORPHINE HYDROCHLORIDEF39049Y068ACTIB
APOMORPHINE HYDROCHLORIDEF39049Y068ACTIB
APOMORPHINE HYDROCHLORIDEF39049Y068ACTIB
APOMORPHINE HYDROCHLORIDEF39049Y068ACTIB

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
apomorphine hydroclorideAPOMORPHINE HYDROCHLORIDETruPharma, LLCaedf70e4-1949-44bc-bf1b-0f282c4f07052022-02-24Warnings, Adverse reactionsName fallback
generic name: APOMORPHINE HYDROCHLORIDE

Reported adverse events (FAERS/openFDA)#

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