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United States · US · US:70771-1651_0bf02fa2-e5cd-42d6-ab41-1ecd150b7c57
Venlafaxine
Orange BookUNIISPLATC N06AX16
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerZydus Lifesciences Limited
CountryUS (United States)
ATC codeN06AX16
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc117077116511100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1651-1)
- ndc11707711651330 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1651-3)
- ndc11707711651990 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1651-9)
Annotations
UNII (FDA Substance ID)
7D7RX5A8MO
VENLAFAXINE HYDROCHLORIDE
RxCUI 235988
Orange Book
A215622
ABABABAB
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": "70771-1651_0bf02fa2-e5cd-42d6-ab41-1ecd150b7c57",
"productndc": "70771-1651",
"dosage_form": "TABLET, EXTENDED RELEASE",
"orange_book": {
"appl_no": "215622",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 37.5MG BASE",
"product_no": "001",
"approval_date": "Aug 30, 2022"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 75MG BASE",
"product_no": "002",
"approval_date": "Aug 30, 2022"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 150MG BASE",
"product_no": "003",
"approval_date": "Aug 30, 2022"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 225MG BASE",
"product_no": "004",
"approval_date": "Aug 30, 2022"
}
],
"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": "ANDA215622",
"marketing_category": "ANDA",
"nonproprietary_name": "Venlafaxine",
"start_marketing_date": "20220901",
"active_numerator_strength": "150"
}Related drugs
Other records sharing ATC code N06AX16.
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