Desvenlafaxine Succinate

Orange BookUNIISPLATC N06AX23

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerBryant Ranch Prepack

CountryUS (United States)

ATC codeN06AX23

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 5

ndc11
7133511501
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1150-1)
ndc11
7133511502
28 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1150-2)
ndc11
7133511503
60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1150-3)
ndc11
7133511504
90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1150-4)
ndc11
7133511505
180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1150-5)

Annotations

UNII (FDA Substance ID)

ZB22ENF0XR

DESVENLAFAXINE SUCCINATE

RxCUI 683693

Orange Book

A204172

ABABAB

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": "71335-1150_540df1fc-389c-44bb-b9bd-b453b57e17c3",
  "productndc": "71335-1150",
  "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE",
  "orange_book": {
    "appl_no": "204172",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 50MG BASE",
        "product_no": "001",
        "approval_date": "Jun 29, 2015"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 100MG BASE",
        "product_no": "002",
        "approval_date": "Jun 29, 2015"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 25MG BASE",
        "product_no": "003",
        "approval_date": "Apr 13, 2022"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "DESVENLAFAXINE SUCCINATE",
  "proprietary_name": "Desvenlafaxine Succinate",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA204172",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Desvenlafaxine Succinate",
  "start_marketing_date": "20170301",
  "active_numerator_strength": "50"
}

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