Venlafaxine
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
- Venlafaxine
- Generic name
- VENLAFAXINE
- Manufacturer
- Zydus Lifesciences Limited
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 750333ce-a512-42e1-b9e3-179714b488df
- SPL ID
- 0bf02fa2-e5cd-42d6-ab41-1ecd150b7c57
- Version
- 2
- Effective date
- 2023-09-28
- Source export date
- 2026-09-28
- Source partition
- 4
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:23:56
| 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 | 215622 | derived:openfda.application_number |
| application number | ANDA215622 | openfda.application_number | |
| brand name | Venlafaxine | openfda.brand_name | |
| generic name | VENLAFAXINE | openfda.generic_name | |
| manufacturer name | Zydus Lifesciences Limited | openfda.manufacturer_name | |
| ndc | package | 70771-1650-1 | openfda.package_ndc |
| ndc | package | 70771-1650-3 | openfda.package_ndc |
| ndc | package | 70771-1651-9 | openfda.package_ndc |
| ndc | package | 70771-1651-3 | openfda.package_ndc |
| ndc | package | 70771-1652-1 | openfda.package_ndc |
| ndc | package | 70771-1652-3 | openfda.package_ndc |
| ndc | package | 70771-1649-3 | openfda.package_ndc |
| ndc | package | 70771-1649-9 | openfda.package_ndc |
| ndc | package | 70771-1651-1 | openfda.package_ndc |
| ndc | package | 70771-1649-1 | openfda.package_ndc |
| ndc | package | 70771-1652-9 | openfda.package_ndc |
| ndc | package | 70771-1650-9 | openfda.package_ndc |
| ndc | product | 70771-1650 | openfda.product_ndc |
| ndc | product | 70771-1652 | openfda.product_ndc |
| ndc | product | 70771-1649 | openfda.product_ndc |
| ndc | product | 70771-1651 | openfda.product_ndc |
| ndc11 | package | 70771165101 | derived:openfda.package_ndc |
| ndc11 | package | 70771165001 | derived:openfda.package_ndc |
| ndc11 | package | 70771165003 | derived:openfda.package_ndc |
| ndc11 | package | 70771165103 | derived:openfda.package_ndc |
| ndc11 | package | 70771164901 | derived:openfda.package_ndc |
| ndc11 | package | 70771165009 | derived:openfda.package_ndc |
| ndc11 | package | 70771165203 | derived:openfda.package_ndc |
| ndc11 | package | 70771165209 | derived:openfda.package_ndc |
| ndc11 | package | 70771165201 | derived:openfda.package_ndc |
| ndc11 | package | 70771164909 | derived:openfda.package_ndc |
| ndc11 | package | 70771164903 | derived:openfda.package_ndc |
| ndc11 | package | 70771165109 | derived:openfda.package_ndc |
| rxcui | 808753 | openfda.rxcui | |
| rxcui | 808751 | openfda.rxcui | |
| rxcui | 808748 | openfda.rxcui | |
| rxcui | 808744 | openfda.rxcui | |
| spl id | 0bf02fa2-e5cd-42d6-ab41-1ecd150b7c57 | id | |
| spl set id | 750333ce-a512-42e1-b9e3-179714b488df | set_id | |
| unii | 7D7RX5A8MO | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.