Haloperidol
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- Haloperidol
- Generic name
- HALOPERIDOL
- Manufacturer
- Zydus Lifesciences Limited
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 509d0eb2-b930-4836-9669-dbebf0ac4076
- SPL ID
- 2ff366f9-878f-4fcb-b2d4-00fb6e31ecbf
- Version
- 8
- Effective date
- 2024-11-30
- Source export date
- 2026-10-12
- Source partition
- 3
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:33:23
| Harmonized routes |
|---|
| ORAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| ndc11 | package | 65841083777 | derived:openfda.package_ndc |
| ndc11 | package | 65841062610 | derived:openfda.package_ndc |
| ndc11 | package | 65841083977 | derived:openfda.package_ndc |
| ndc11 | package | 65841083877 | derived:openfda.package_ndc |
| ndc11 | package | 65841062601 | derived:openfda.package_ndc |
| ndc11 | package | 65841062801 | derived:openfda.package_ndc |
| ndc11 | package | 65841083810 | derived:openfda.package_ndc |
| rxcui | 314035 | openfda.rxcui | |
| rxcui | 314034 | openfda.rxcui | |
| rxcui | 310670 | openfda.rxcui | |
| rxcui | 310672 | openfda.rxcui | |
| rxcui | 310671 | openfda.rxcui | |
| rxcui | 197754 | openfda.rxcui | |
| spl id | 2ff366f9-878f-4fcb-b2d4-00fb6e31ecbf | id | |
| spl set id | 509d0eb2-b930-4836-9669-dbebf0ac4076 | set_id | |
| unii | J6292F8L3D | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.