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United States · US · US:71335-2651_aa842ba3-79c6-4dbc-888e-31b36c5dabe5

Trazodone Hydrochloride

Orange BookUNIISPLATC N06AX05

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

Identification

ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeN06AX05
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 10

  • ndc11
    7133526510
    14 TABLET in 1 BOTTLE (71335-2651-0)
  • ndc11
    7133526511
    20 TABLET in 1 BOTTLE (71335-2651-1)
  • ndc11
    7133526512
    30 TABLET in 1 BOTTLE (71335-2651-2)
  • ndc11
    7133526513
    60 TABLET in 1 BOTTLE (71335-2651-3)
  • ndc11
    7133526514
    90 TABLET in 1 BOTTLE (71335-2651-4)
  • ndc11
    7133526515
    45 TABLET in 1 BOTTLE (71335-2651-5)
  • ndc11
    7133526516
    100 TABLET in 1 BOTTLE (71335-2651-6)
  • ndc11
    7133526517
    25 TABLET in 1 BOTTLE (71335-2651-7)
  • ndc11
    7133526518
    120 TABLET in 1 BOTTLE (71335-2651-8)
  • ndc11
    7133526519
    28 TABLET in 1 BOTTLE (71335-2651-9)

Annotations

UNII (FDA Substance ID)
6E8ZO8LRNM
TRAZODONE HYDROCHLORIDE
RxCUI 82112
Orange Book
A202180
ABABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "6E8ZO8LRNM",
    "rxcui": "82112",
    "inchikey": "OHHDIOKRWWOXMT-UHFFFAOYSA-N",
    "display_name": "TRAZODONE HYDROCHLORIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "df17cec9-ad5e-4e57-8572-c927c9b955e2": {
      "match": "brand_token",
      "title": "TRAZODONE HYDROCHLORIDE TABLET [NCS HEALTHCARE OF KY, LLC DBA VANGARD LABS]",
      "spl_version": "30",
      "published_date": "2026-05-29"
    }
  },
  "productid": "71335-2651_aa842ba3-79c6-4dbc-888e-31b36c5dabe5",
  "productndc": "71335-2651",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "202180",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "50MG",
        "product_no": "001",
        "approval_date": "Nov 27, 2013"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "100MG",
        "product_no": "002",
        "approval_date": "Nov 27, 2013"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "150MG",
        "product_no": "003",
        "approval_date": "Nov 27, 2013"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "300MG",
        "product_no": "004",
        "approval_date": "Nov 27, 2013"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "TRAZODONE HYDROCHLORIDE",
  "proprietary_name": "Trazodone Hydrochloride",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA202180",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Trazodone Hydrochloride",
  "start_marketing_date": "20131127",
  "active_numerator_strength": "50"
}

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