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United States · US · US:70010-186_4f19b9ad-53a9-da61-e063-6294a90afadf
Venlafaxine Hydrochloride
Orange BookUNIISPLATC N06AX16
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerGranules Pharmaceuticals Inc.
CountryUS (United States)
ATC codeN06AX16
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 6
- ndc11700101860330 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70010-186-03)
- ndc117001018605500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70010-186-05)
- ndc11700101860990 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70010-186-09)
- ndc1170010186101000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70010-186-10)
- ndc11700101863315 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70010-186-33)
- ndc1170010186638 BLISTER PACK in 1 CARTON (70010-186-63) / 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK
Annotations
UNII (FDA Substance ID)
7D7RX5A8MO
VENLAFAXINE HYDROCHLORIDE
RxCUI 235988
Orange Book
A217390
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": "70010-186_4f19b9ad-53a9-da61-e063-6294a90afadf",
"productndc": "70010-186",
"dosage_form": "CAPSULE, EXTENDED RELEASE",
"orange_book": {
"appl_no": "217390",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 37.5MG BASE",
"product_no": "001",
"approval_date": "May 18, 2023"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 75MG BASE",
"product_no": "002",
"approval_date": "May 18, 2023"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 150MG BASE",
"product_no": "003",
"approval_date": "May 18, 2023"
}
],
"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": "ANDA217390",
"marketing_category": "ANDA",
"nonproprietary_name": "Venlafaxine Hydrochloride",
"start_marketing_date": "20230925",
"active_numerator_strength": "150"
}Related drugs
Other records sharing ATC code N06AX16.
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