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 (canonical bytes are SHA-256 checked before publication)

Brand name
Venlafaxine Hydrochloride
Generic name
VENLAFAXINE HYDROCHLORIDE
Manufacturer
Zydus Lifesciences Limited
Product type
HUMAN PRESCRIPTION DRUG
SPL set ID
51334651-7a7f-4653-bf9d-d5be04fd902d
SPL ID
d4325db5-166d-4719-bdbd-a89ef8c96833
Version
10
Effective date
2024-08-14
Source export date
2026-10-27
Source partition
12
Source file
https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-27/977776a6cc37ec1c77259da8a93ae161850a3aa120341096e5a03428b84d016b/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run
20261027T193451Z
Imported at
2026-10-27 21:01:47
Harmonized routes table
Harmonized routes
ORAL

Reported adverse events (FAERS/openFDA)#

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