Paroxetine
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
- Paroxetine
- Generic name
- PAROXETINE HYDROCHLORIDE
- Manufacturer
- Zydus Lifesciences Limited
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 6d5fcdb2-4d84-4b20-87e3-58a43e567500
- SPL ID
- ef5c1ef5-2884-4395-a65a-92591c986150
- Version
- 13
- Effective date
- 2024-12-03
- Source export date
- 2026-11-06
- Source partition
- 8
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-11-06/db89d5ebfc3e02f44e8769334d799cd3436b05f779823ab00297f1f800c89ddf/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
- Import run
- 20261108T063105Z
- Imported at
- 2026-11-08 07:32:09
| 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 |
|---|---|---|---|
| application applno | ANDA | 077584 | derived:openfda.application_number |
| application number | ANDA077584 | openfda.application_number | |
| brand name | Paroxetine | openfda.brand_name | |
| generic name | PAROXETINE HYDROCHLORIDE | openfda.generic_name | |
| manufacturer name | Zydus Lifesciences Limited | openfda.manufacturer_name | |
| ndc | package | 65841-099-10 | openfda.package_ndc |
| ndc | package | 65841-097-10 | openfda.package_ndc |
| ndc | package | 65841-099-05 | openfda.package_ndc |
| ndc | package | 65841-601-10 | openfda.package_ndc |
| ndc | package | 65841-097-16 | openfda.package_ndc |
| ndc | package | 65841-099-16 | openfda.package_ndc |
| ndc | package | 65841-099-01 | openfda.package_ndc |
| ndc | package | 65841-601-05 | openfda.package_ndc |
| ndc | package | 65841-098-06 | openfda.package_ndc |
| ndc | package | 65841-097-01 | openfda.package_ndc |
| ndc | package | 65841-601-01 | openfda.package_ndc |
| ndc | package | 65841-097-05 | openfda.package_ndc |
| ndc | package | 65841-601-16 | openfda.package_ndc |
| ndc | package | 65841-098-01 | openfda.package_ndc |
| ndc | package | 65841-098-10 | openfda.package_ndc |
| ndc | package | 65841-098-16 | openfda.package_ndc |
| ndc | package | 65841-601-06 | openfda.package_ndc |
| ndc | package | 65841-097-06 | openfda.package_ndc |
| ndc | package | 65841-098-05 | openfda.package_ndc |
| ndc | package | 65841-099-06 | openfda.package_ndc |
| ndc | product | 65841-097 | openfda.product_ndc |
| ndc | product | 65841-601 | openfda.product_ndc |
| ndc | product | 65841-098 | openfda.product_ndc |
| ndc | product | 65841-099 | openfda.product_ndc |
| ndc11 | package | 65841060101 | derived:openfda.package_ndc |
| ndc11 | package | 65841009806 | derived:openfda.package_ndc |
| ndc11 | package | 65841009705 | derived:openfda.package_ndc |
| ndc11 | package | 65841009701 | derived:openfda.package_ndc |
| ndc11 | package | 65841009905 | derived:openfda.package_ndc |
| ndc11 | package | 65841060110 | derived:openfda.package_ndc |
| ndc11 | package | 65841009710 | derived:openfda.package_ndc |
| ndc11 | package | 65841009916 | derived:openfda.package_ndc |
| ndc11 | package | 65841060116 | derived:openfda.package_ndc |
| ndc11 | package | 65841009716 | derived:openfda.package_ndc |
| ndc11 | package | 65841009805 | derived:openfda.package_ndc |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.