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United States · US · US:71335-9605_cf86ed39-0f0a-4666-a225-9c50044e249e
Venlafaxine Hydrochloride
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 · 5
- ndc11713359605130 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-9605-1)
- ndc11713359605260 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-9605-2)
- ndc11713359605310 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-9605-3)
- ndc11713359605490 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-9605-4)
- ndc11713359605514 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-9605-5)
Annotations
UNII (FDA Substance ID)
7D7RX5A8MO
VENLAFAXINE HYDROCHLORIDE
RxCUI 235988
Orange Book
A212277
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": "71335-9605_cf86ed39-0f0a-4666-a225-9c50044e249e",
"productndc": "71335-9605",
"dosage_form": "CAPSULE, EXTENDED RELEASE",
"orange_book": {
"appl_no": "212277",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 37.5MG BASE",
"product_no": "001",
"approval_date": "Jul 8, 2019"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 75MG BASE",
"product_no": "002",
"approval_date": "Jul 8, 2019"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 150MG BASE",
"product_no": "003",
"approval_date": "Jul 8, 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": "ANDA212277",
"marketing_category": "ANDA",
"nonproprietary_name": "Venlafaxine Hydrochloride",
"start_marketing_date": "20190708",
"active_numerator_strength": "37.5"
}Related drugs
Other records sharing ATC code N06AX16.
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