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United States · US · US:62332-233_d97cafa3-ede7-49c6-bba1-6414e6968cb5

VILAZODONE HYDROCHLORIDE

Orange BookUNIISPLATC N06AX24

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerAlembic Pharmaceuticals Inc.
CountryUS (United States)
ATC codeN06AX24
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 4

  • ndc11
    6233223330
    30 TABLET, FILM COATED in 1 BOTTLE (62332-233-30)
  • ndc11
    6233223371
    500 TABLET, FILM COATED in 1 BOTTLE (62332-233-71)
  • ndc11
    6233223390
    90 TABLET, FILM COATED in 1 BOTTLE (62332-233-90)
  • ndc11
    6233223391
    1000 TABLET, FILM COATED in 1 BOTTLE (62332-233-91)

Annotations

UNII (FDA Substance ID)
U8HTX2GK8J
VILAZODONE HYDROCHLORIDE
RxCUI 1086768
Orange Book
A208202
ABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "U8HTX2GK8J",
    "rxcui": "1086768",
    "inchikey": "RPZBRGFNBNQSOP-UHFFFAOYSA-N",
    "display_name": "VILAZODONE HYDROCHLORIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "061efdcc-40ea-4647-8cc8-01cd1ccca68b": {
      "match": "brand_token",
      "title": "VILAZODONE HYDROCHLORIDE TABLET [PREFERRED PHARMACEUTICALS INC.]",
      "spl_version": "2",
      "published_date": "2025-11-17"
    }
  },
  "productid": "62332-233_d97cafa3-ede7-49c6-bba1-6414e6968cb5",
  "productndc": "62332-233",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "208202",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "10MG",
        "product_no": "001",
        "approval_date": "Jan 10, 2020"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "20MG",
        "product_no": "002",
        "approval_date": "Jan 10, 2020"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "40MG",
        "product_no": "003",
        "approval_date": "Jan 10, 2020"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "VILAZODONE HYDROCHLORIDE",
  "proprietary_name": "VILAZODONE HYDROCHLORIDE",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA208202",
  "marketing_category": "ANDA",
  "nonproprietary_name": "VILAZODONE HYDROCHLORIDE",
  "start_marketing_date": "20220604",
  "active_numerator_strength": "20"
}

Related drugs

Other records sharing ATC code N06AX24.

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