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United States · US · US:63304-192_cd04a0b2-a7f2-4629-997f-af2a8e65f15b
Desvenlafaxine
Orange BookUNIISPLATC N06AX23
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerSun Pharmaceutical Industries, Inc.
CountryUS (United States)
ATC codeN06AX23
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc11633041923030 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-192-30)
- ndc11633041929090 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-192-90)
Annotations
UNII (FDA Substance ID)
NG99554ANW
DESVENLAFAXINE
RxCUI 734064
Orange Book
N204150
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "NG99554ANW",
"rxcui": "734064",
"inchikey": "KYYIDSXMWOZKMP-UHFFFAOYSA-N",
"display_name": "DESVENLAFAXINE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"1d8889c9-9403-4b4b-8abd-7dc9a9fc1816": {
"match": "brand_token",
"title": "DESVENLAFAXINE TABLET, EXTENDED RELEASE [BRYANT RANCH PREPACK]",
"spl_version": "107",
"published_date": "2026-05-25"
}
},
"productid": "63304-192_cd04a0b2-a7f2-4629-997f-af2a8e65f15b",
"productndc": "63304-192",
"dosage_form": "TABLET, EXTENDED RELEASE",
"orange_book": {
"appl_no": "204150",
"products": [
{
"rs": false,
"rld": true,
"te_code": null,
"strength": "50MG",
"product_no": "001",
"approval_date": "Mar 4, 2013"
},
{
"rs": true,
"rld": true,
"te_code": null,
"strength": "100MG",
"product_no": "002",
"approval_date": "Mar 4, 2013"
}
],
"appl_type": "N"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "DESVENLAFAXINE",
"proprietary_name": "Desvenlafaxine",
"active_ingred_unit": "mg/1",
"application_number": "NDA204150",
"marketing_category": "NDA",
"nonproprietary_name": "Desvenlafaxine",
"start_marketing_date": "20130305",
"active_numerator_strength": "100"
}Related drugs
Other records sharing ATC code N06AX23.
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