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United States · US · US:62332-011_8724b94d-b3fd-4844-a7fe-2be7982cf8f5
venlafaxine
Orange BookUNIISPLATC N06AX16
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAlembic Pharmaceuticals Inc.
CountryUS (United States)
ATC codeN06AX16
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc11623320113030 TABLET in 1 BOTTLE (62332-011-30)
- ndc116233201131100 TABLET in 1 BOTTLE (62332-011-31)
- ndc1162332011911000 TABLET in 1 BOTTLE (62332-011-91)
Annotations
UNII (FDA Substance ID)
7D7RX5A8MO
VENLAFAXINE HYDROCHLORIDE
RxCUI 235988
Orange Book
A078932
ABABABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "7D7RX5A8MO",
"rxcui": "235988",
"inchikey": "QYRYFNHXARDNFZ-UHFFFAOYSA-N",
"display_name": "VENLAFAXINE HYDROCHLORIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"b865c175-e75d-4cb4-ac29-dec72226302c": {
"match": "brand_token",
"title": "VENLAFAXINE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE [NORTHSTAR RXLLC]",
"spl_version": "1",
"published_date": "2026-06-02"
}
},
"productid": "62332-011_8724b94d-b3fd-4844-a7fe-2be7982cf8f5",
"productndc": "62332-011",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "078932",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 25MG BASE",
"product_no": "001",
"approval_date": "Dec 14, 2010"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 37.5MG BASE",
"product_no": "002",
"approval_date": "Dec 14, 2010"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 50MG BASE",
"product_no": "003",
"approval_date": "Dec 14, 2010"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 75MG BASE",
"product_no": "004",
"approval_date": "Dec 14, 2010"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 100MG BASE",
"product_no": "005",
"approval_date": "Dec 14, 2010"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "VENLAFAXINE HYDROCHLORIDE",
"proprietary_name": "venlafaxine",
"active_ingred_unit": "mg/1",
"application_number": "ANDA078932",
"marketing_category": "ANDA",
"nonproprietary_name": "venlafaxine",
"start_marketing_date": "20151001",
"active_numerator_strength": "75"
}Related drugs
Other records sharing ATC code N06AX16.
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