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United States · US · US:33342-194_ea9c3795-420f-49fb-918c-7033a1f06963
Venlafaxine hydrochloride
Orange BookUNIISPLATC N06AX16
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerMacleods Pharmaceuticals Limited
CountryUS (United States)
ATC codeN06AX16
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 5
- ndc11333421940730 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (33342-194-07)
- ndc11333421941090 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (33342-194-10)
- ndc113334219411100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (33342-194-11)
- ndc11333421941210 BLISTER PACK in 1 CARTON (33342-194-12) / 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK
- ndc113334219415500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (33342-194-15)
Annotations
UNII (FDA Substance ID)
7D7RX5A8MO
VENLAFAXINE HYDROCHLORIDE
RxCUI 235988
Orange Book
A204889
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": {
"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": "33342-194_ea9c3795-420f-49fb-918c-7033a1f06963",
"productndc": "33342-194",
"dosage_form": "CAPSULE, EXTENDED RELEASE",
"orange_book": {
"appl_no": "204889",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 37.5MG BASE",
"product_no": "001",
"approval_date": "Oct 5, 2017"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 75MG BASE",
"product_no": "002",
"approval_date": "Oct 5, 2017"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 150MG BASE",
"product_no": "003",
"approval_date": "Oct 5, 2017"
}
],
"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": "ANDA204889",
"marketing_category": "ANDA",
"nonproprietary_name": "Venlafaxine hydrochloride",
"start_marketing_date": "20171006",
"active_numerator_strength": "37.5"
}Related drugs
Other records sharing ATC code N06AX16.
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