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United States · US · US:62135-531_45adb66f-add1-678a-e063-6394a90a1f26
venlafaxine hydrochloride
Orange BookUNIISPLATC N06AX16
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerChartwell RX, LLC
CountryUS (United States)
ATC codeN06AX16
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11621355313030 TABLET in 1 BOTTLE (62135-531-30)
Annotations
UNII (FDA Substance ID)
7D7RX5A8MO
VENLAFAXINE HYDROCHLORIDE
RxCUI 235988
Orange Book
A209193
ABAB
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": "62135-531_45adb66f-add1-678a-e063-6394a90a1f26",
"productndc": "62135-531",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "209193",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 150MG BASE",
"product_no": "001",
"approval_date": "Oct 31, 2019"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 225MG BASE",
"product_no": "002",
"approval_date": "Oct 31, 2019"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "VENLAFAXINE HYDROCHLORIDE",
"proprietary_name": "venlafaxine hydrochloride",
"active_ingred_unit": "mg/1",
"application_number": "ANDA209193",
"marketing_category": "ANDA",
"nonproprietary_name": "venlafaxine hydrochloride",
"start_marketing_date": "20191226",
"active_numerator_strength": "225"
}Related drugs
Other records sharing ATC code N06AX16.
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