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United States · US · US:71785-1007_b45cbdea-d1be-c16d-e053-2a95a90a821e
VENLAFAXINE HYDROCHLORIDE
Orange BookUNIISPLATC N06AX16
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAnnora Pharma Private Limited
CountryUS (United States)
ATC codeN06AX16
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 4
- ndc11717851007030 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71785-1007-0)
- ndc11717851007190 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71785-1007-1)
- ndc117178510072500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71785-1007-2)
- ndc11717851007310 BLISTER PACK in 1 CARTON (71785-1007-3) / 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK
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": "71785-1007_b45cbdea-d1be-c16d-e053-2a95a90a821e",
"productndc": "71785-1007",
"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": "75"
}Related drugs
Other records sharing ATC code N06AX16.
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