Nefazodone Hydrochloride

Orange BookUNIISPLATC N06AX06

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

Identification

ManufacturerTeva Pharmaceuticals USA, Inc.

CountryUS (United States)

ATC codeN06AX06

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
0093102406
60 TABLET in 1 BOTTLE (0093-1024-06)

Annotations

UNII (FDA Substance ID)

27X63J94GR

NEFAZODONE HYDROCHLORIDE

RxCUI 236082

Orange Book

A076037

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "27X63J94GR",
    "rxcui": "236082",
    "inchikey": "DYCKFEBIOUQECE-UHFFFAOYSA-N",
    "display_name": "NEFAZODONE HYDROCHLORIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "51ff7db5-aaf9-4c3c-86e6-958ebf16b60f": {
      "match": "brand_token",
      "title": "NEFAZODONE HYDROCHLORIDE TABLET [TEVA PHARMACEUTICALS USA, INC.]",
      "spl_version": "12",
      "published_date": "2025-11-17"
    }
  },
  "productid": "0093-1024_11cdc932-271c-4988-aad9-076340888bce",
  "productndc": "0093-1024",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "076037",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "50MG",
        "product_no": "001",
        "approval_date": "Sep 16, 2003"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "100MG",
        "product_no": "002",
        "approval_date": "Sep 16, 2003"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "150MG",
        "product_no": "003",
        "approval_date": "Sep 16, 2003"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "200MG",
        "product_no": "004",
        "approval_date": "Sep 16, 2003"
      },
      {
        "rs": true,
        "rld": false,
        "te_code": null,
        "strength": "250MG",
        "product_no": "005",
        "approval_date": "Sep 16, 2003"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "NEFAZODONE HYDROCHLORIDE",
  "proprietary_name": "Nefazodone Hydrochloride",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA076037",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Nefazodone Hydrochloride",
  "start_marketing_date": "20030916",
  "active_numerator_strength": "100"
}

Related drugs

Other records sharing ATC code N06AX06.

Access this data programmatically

Query Nefazodone Hydrochloride and 610,000+ other drug records through a single REST API — with a last_synced_at provenance stamp on every response. Free tier includes 100 requests/day.

Get a free API key Read the API docs