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United States · US · US:71335-0705_37651ec2-0d18-3c66-e063-6294a90afbdb

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
    7133507050
    14 TABLET in 1 BOTTLE (71335-0705-0)
  • ndc11
    7133507051
    20 TABLET in 1 BOTTLE (71335-0705-1)
  • ndc11
    7133507052
    30 TABLET in 1 BOTTLE (71335-0705-2)
  • ndc11
    7133507053
    60 TABLET in 1 BOTTLE (71335-0705-3)
  • ndc11
    7133507054
    90 TABLET in 1 BOTTLE (71335-0705-4)
  • ndc11
    7133507055
    45 TABLET in 1 BOTTLE (71335-0705-5)
  • ndc11
    7133507056
    100 TABLET in 1 BOTTLE (71335-0705-6)
  • ndc11
    7133507057
    25 TABLET in 1 BOTTLE (71335-0705-7)
  • ndc11
    7133507058
    120 TABLET in 1 BOTTLE (71335-0705-8)
  • ndc11
    7133507059
    28 TABLET in 1 BOTTLE (71335-0705-9)

Annotations

UNII (FDA Substance ID)
6E8ZO8LRNM
TRAZODONE HYDROCHLORIDE
RxCUI 82112
Orange Book
A205253
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": "71335-0705_37651ec2-0d18-3c66-e063-6294a90afbdb",
  "productndc": "71335-0705",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "205253",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "50MG",
        "product_no": "001",
        "approval_date": "Oct 10, 2017"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "100MG",
        "product_no": "002",
        "approval_date": "Oct 10, 2017"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "150MG",
        "product_no": "003",
        "approval_date": "Oct 10, 2017"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "300MG",
        "product_no": "004",
        "approval_date": "Oct 10, 2017"
      }
    ],
    "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": "ANDA205253",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Trazodone Hydrochloride",
  "start_marketing_date": "20171211",
  "active_numerator_strength": "50"
}

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