venlafaxine hydrochloride
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 hydrochloride
- Generic name
- VENLAFAXINE HYDROCHLORIDE
- Manufacturer
- Zydus Lifesciences Limited
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 1be1be3a-304b-4e31-8732-335247029191
- SPL ID
- f20749dc-d1f6-4860-b583-82b82d3a2242
- Version
- 10
- Effective date
- 2023-09-28
- Source export date
- 2026-09-28
- Source partition
- 11
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:18:57
| 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 | 090174 | derived:openfda.application_number |
| application number | ANDA090174 | openfda.application_number | |
| brand name | venlafaxine hydrochloride | openfda.brand_name | |
| generic name | VENLAFAXINE HYDROCHLORIDE | openfda.generic_name | |
| manufacturer name | Zydus Lifesciences Limited | openfda.manufacturer_name | |
| ndc | package | 65841-751-10 | openfda.package_ndc |
| ndc | package | 65841-751-06 | openfda.package_ndc |
| ndc | package | 65841-753-10 | openfda.package_ndc |
| ndc | package | 65841-752-06 | openfda.package_ndc |
| ndc | package | 65841-753-16 | openfda.package_ndc |
| ndc | package | 65841-751-16 | openfda.package_ndc |
| ndc | package | 65841-753-06 | openfda.package_ndc |
| ndc | package | 65841-752-16 | openfda.package_ndc |
| ndc | package | 65841-752-10 | openfda.package_ndc |
| ndc | product | 65841-752 | openfda.product_ndc |
| ndc | product | 65841-751 | openfda.product_ndc |
| ndc | product | 65841-753 | openfda.product_ndc |
| ndc11 | package | 65841075210 | derived:openfda.package_ndc |
| ndc11 | package | 65841075316 | derived:openfda.package_ndc |
| ndc11 | package | 65841075216 | derived:openfda.package_ndc |
| ndc11 | package | 65841075206 | derived:openfda.package_ndc |
| ndc11 | package | 65841075116 | derived:openfda.package_ndc |
| ndc11 | package | 65841075106 | derived:openfda.package_ndc |
| ndc11 | package | 65841075306 | derived:openfda.package_ndc |
| ndc11 | package | 65841075310 | derived:openfda.package_ndc |
| ndc11 | package | 65841075110 | derived:openfda.package_ndc |
| rxcui | 313585 | openfda.rxcui | |
| rxcui | 313583 | openfda.rxcui | |
| rxcui | 313581 | openfda.rxcui | |
| spl id | f20749dc-d1f6-4860-b583-82b82d3a2242 | id | |
| spl set id | 1be1be3a-304b-4e31-8732-335247029191 | set_id | |
| unii | 7D7RX5A8MO | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.