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United States · US · US:71335-9704_1471508e-7fe4-43db-94ea-b4df1bcbafa9
Venlafaxine
Orange BookUNIISPLATC N06AX16
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeN06AX16
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 4
- ndc11713359704130 TABLET in 1 BOTTLE (71335-9704-1)
- ndc11713359704260 TABLET in 1 BOTTLE (71335-9704-2)
- ndc11713359704390 TABLET in 1 BOTTLE (71335-9704-3)
- ndc11713359704410 TABLET in 1 BOTTLE (71335-9704-4)
Annotations
UNII (FDA Substance ID)
7D7RX5A8MO
VENLAFAXINE HYDROCHLORIDE
RxCUI 235988
Orange Book
A077653
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": "71335-9704_1471508e-7fe4-43db-94ea-b4df1bcbafa9",
"productndc": "71335-9704",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "077653",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 25MG BASE",
"product_no": "001",
"approval_date": "Jun 13, 2008"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 37.5MG BASE",
"product_no": "002",
"approval_date": "Jun 13, 2008"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 50MG BASE",
"product_no": "003",
"approval_date": "Jun 13, 2008"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 75MG BASE",
"product_no": "004",
"approval_date": "Jun 13, 2008"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 100MG BASE",
"product_no": "005",
"approval_date": "Jun 13, 2008"
}
],
"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": "ANDA077653",
"marketing_category": "ANDA",
"nonproprietary_name": "Venlafaxine",
"start_marketing_date": "20080613",
"active_numerator_strength": "37.5"
}Related drugs
Other records sharing ATC code N06AX16.
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