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United States · US · US:43598-944_79d34297-6604-4031-a89a-8ec557d078d1
Venlafaxine
Orange BookUNIISPLATC N06AX16
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerDr. Reddy's Laboratories Inc.
CountryUS (United States)
ATC codeN06AX16
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc11435989443030 TABLET, EXTENDED RELEASE in 1 BOTTLE (43598-944-30)
- ndc11435989449090 TABLET, EXTENDED RELEASE in 1 BOTTLE (43598-944-90)
Annotations
UNII (FDA Substance ID)
7D7RX5A8MO
VENLAFAXINE HYDROCHLORIDE
RxCUI 235988
Orange Book
A214609
ABAB
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": "43598-944_79d34297-6604-4031-a89a-8ec557d078d1",
"productndc": "43598-944",
"dosage_form": "TABLET, EXTENDED RELEASE",
"orange_book": {
"appl_no": "214609",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 150MG BASE",
"product_no": "001",
"approval_date": "Jun 30, 2021"
},
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 225MG BASE",
"product_no": "002",
"approval_date": "Jun 30, 2021"
}
],
"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": "ANDA214609",
"marketing_category": "ANDA",
"nonproprietary_name": "Venlafaxine",
"start_marketing_date": "20210920",
"active_numerator_strength": "225"
}Related drugs
Other records sharing ATC code N06AX16.
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