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United States · US · US:71335-1753_3dd007f9-261b-47e8-8dfc-d92ffdd2f430

Desvenlafaxine

Orange BookUNIISPLATC 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

  • ndc11
    7133517531
    30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1753-1)
  • ndc11
    7133517532
    28 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1753-2)
  • ndc11
    7133517533
    60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1753-3)
  • ndc11
    7133517534
    90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1753-4)
  • ndc11
    7133517535
    180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1753-5)

Annotations

UNII (FDA Substance ID)
ZB22ENF0XR
DESVENLAFAXINE SUCCINATE
RxCUI 683693
Orange Book
A210014
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": "71335-1753_3dd007f9-261b-47e8-8dfc-d92ffdd2f430",
  "productndc": "71335-1753",
  "dosage_form": "TABLET, EXTENDED RELEASE",
  "orange_book": {
    "appl_no": "210014",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 50MG BASE",
        "product_no": "001",
        "approval_date": "Oct 1, 2018"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 100MG BASE",
        "product_no": "002",
        "approval_date": "Oct 1, 2018"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 25MG BASE",
        "product_no": "003",
        "approval_date": "Oct 13, 2020"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "DESVENLAFAXINE SUCCINATE",
  "proprietary_name": "Desvenlafaxine",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA210014",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Desvenlafaxine",
  "start_marketing_date": "20200801",
  "active_numerator_strength": "50"
}

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