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United States · US · US:71335-3112_56e6b3ed-ecc8-486c-8ef0-d4e474553c27

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 · 7

  • ndc11
    7133531121
    30 TABLET in 1 BOTTLE (71335-3112-1)
  • ndc11
    7133531122
    60 TABLET in 1 BOTTLE (71335-3112-2)
  • ndc11
    7133531123
    90 TABLET in 1 BOTTLE (71335-3112-3)
  • ndc11
    7133531124
    18 TABLET in 1 BOTTLE (71335-3112-4)
  • ndc11
    7133531125
    100 TABLET in 1 BOTTLE (71335-3112-5)
  • ndc11
    7133531126
    45 TABLET in 1 BOTTLE (71335-3112-6)
  • ndc11
    7133531127
    180 TABLET in 1 BOTTLE (71335-3112-7)

Annotations

UNII (FDA Substance ID)
6E8ZO8LRNM
TRAZODONE HYDROCHLORIDE
RxCUI 82112
Orange Book
A204852
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": "71335-3112_56e6b3ed-ecc8-486c-8ef0-d4e474553c27",
  "productndc": "71335-3112",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "204852",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "50MG",
        "product_no": "001",
        "approval_date": "Feb 5, 2020"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "100MG",
        "product_no": "002",
        "approval_date": "Feb 5, 2020"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "150MG",
        "product_no": "003",
        "approval_date": "Feb 5, 2020"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "300MG",
        "product_no": "004",
        "approval_date": "Feb 5, 2020"
      }
    ],
    "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": "ANDA204852",
  "marketing_category": "ANDA",
  "nonproprietary_name": "TRAZODONE HYDROCHLORIDE",
  "start_marketing_date": "20150915",
  "active_numerator_strength": "150"
}

Related drugs

Other records sharing ATC code N06AX05.

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