Nefazodone Hydrochloride

Orange BookUNIISPLATC N06AX06

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

Identification

ManufacturerBryant Ranch Prepack

CountryUS (United States)

ATC codeN06AX06

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 4

ndc11
6362970461
30 TABLET in 1 BOTTLE (63629-7046-1)
ndc11
6362970462
120 TABLET in 1 BOTTLE (63629-7046-2)
ndc11
6362970463
28 TABLET in 1 BOTTLE (63629-7046-3)
ndc11
6362970464
60 TABLET in 1 BOTTLE (63629-7046-4)

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": "63629-7046_8962e4a7-1e27-4a03-ab51-34fc4f9c6847",
  "productndc": "63629-7046",
  "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": "150"
}

Related drugs

Other records sharing ATC code N06AX06.

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