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United States · US · US:71335-1700_4a9487ae-3632-40da-b2a7-238060205a74
Desvenlafaxine
UNIISPLATC N06AX23
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeN06AX23
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 5
- ndc11713351700130 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1700-1)
- ndc11713351700228 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1700-2)
- ndc11713351700360 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1700-3)
- ndc11713351700490 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1700-4)
- ndc117133517005180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1700-5)
Annotations
UNII (FDA Substance ID)
ZB22ENF0XR
DESVENLAFAXINE SUCCINATE
RxCUI 683693
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "ZB22ENF0XR",
"rxcui": "683693",
"inchikey": "PWPDEXVGKDEKTE-UHFFFAOYSA-N",
"display_name": "DESVENLAFAXINE SUCCINATE",
"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": "71335-1700_4a9487ae-3632-40da-b2a7-238060205a74",
"productndc": "71335-1700",
"dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE",
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "DESVENLAFAXINE SUCCINATE",
"proprietary_name": "Desvenlafaxine",
"active_ingred_unit": "mg/1",
"application_number": "ANDA204082",
"marketing_category": "ANDA",
"nonproprietary_name": "Desvenlafaxine",
"start_marketing_date": "20170301",
"active_numerator_strength": "50"
}Related drugs
Other records sharing ATC code N06AX23.
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