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United States · US · US:58151-127_2319042f-5d24-42d3-9b0a-8893bed66813
Effexor
Orange BookUNIISPLATC N06AX16
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerViatris Specialty LLC
CountryUS (United States)
ATC codeN06AX16
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc11581511277790 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (58151-127-77)
- ndc11581511279330 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (58151-127-93)
Annotations
UNII (FDA Substance ID)
7D7RX5A8MO
VENLAFAXINE HYDROCHLORIDE
RxCUI 235988
Orange Book
N020699
ABABAB
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": {
"53c3e7ac-1852-4d70-d2b6-4fca819acf26": {
"match": "brand_token",
"title": "EFFEXOR XR (VENLAFAXINE HYDROCHLORIDE) CAPSULE, EXTENDED RELEASE [WYETH PHARMACEUTICALS LLC, A SUBSIDIARY OF PFIZER INC.]",
"spl_version": "50",
"published_date": "2025-07-04"
}
},
"productid": "58151-127_2319042f-5d24-42d3-9b0a-8893bed66813",
"productndc": "58151-127",
"dosage_form": "CAPSULE, EXTENDED RELEASE",
"orange_book": {
"appl_no": "020699",
"products": [
{
"rs": false,
"rld": true,
"te_code": "AB",
"strength": "EQ 37.5MG BASE",
"product_no": "001",
"approval_date": "Oct 20, 1997"
},
{
"rs": false,
"rld": true,
"te_code": "AB",
"strength": "EQ 75MG BASE",
"product_no": "002",
"approval_date": "Oct 20, 1997"
},
{
"rs": false,
"rld": true,
"te_code": null,
"strength": "EQ 100MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**",
"product_no": "003",
"approval_date": "Oct 20, 1997"
},
{
"rs": true,
"rld": true,
"te_code": "AB",
"strength": "EQ 150MG BASE",
"product_no": "004",
"approval_date": "Oct 20, 1997"
}
],
"appl_type": "N"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "VENLAFAXINE HYDROCHLORIDE",
"proprietary_name": "Effexor",
"active_ingred_unit": "mg/1",
"application_number": "NDA020699",
"marketing_category": "NDA",
"nonproprietary_name": "VENLAFAXINE HYDROCHLORIDE",
"start_marketing_date": "20240801",
"active_numerator_strength": "150"
}Related drugs
Other records sharing ATC code N06AX16.
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