Trazodone Hydrochloride

Orange BookUNIISPLATC N06AX05

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

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
7133515750
14 TABLET in 1 BOTTLE (71335-1575-0)
ndc11
7133515751
20 TABLET in 1 BOTTLE (71335-1575-1)
ndc11
7133515752
30 TABLET in 1 BOTTLE (71335-1575-2)
ndc11
7133515753
60 TABLET in 1 BOTTLE (71335-1575-3)
ndc11
7133515754
90 TABLET in 1 BOTTLE (71335-1575-4)
ndc11
7133515755
45 TABLET in 1 BOTTLE (71335-1575-5)
ndc11
7133515756
100 TABLET in 1 BOTTLE (71335-1575-6)
ndc11
7133515757
25 TABLET in 1 BOTTLE (71335-1575-7)
ndc11
7133515758
120 TABLET in 1 BOTTLE (71335-1575-8)
ndc11
7133515759
28 TABLET in 1 BOTTLE (71335-1575-9)

Annotations

UNII (FDA Substance ID)

6E8ZO8LRNM

TRAZODONE HYDROCHLORIDE

RxCUI 82112

Orange Book

A206923

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": "71335-1575_ee5038da-8c02-4fd4-9034-e58f1f3d8e38",
  "productndc": "71335-1575",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "206923",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "50MG",
        "product_no": "001",
        "approval_date": "Sep 8, 2017"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "100MG",
        "product_no": "002",
        "approval_date": "Sep 8, 2017"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "150MG",
        "product_no": "003",
        "approval_date": "Sep 8, 2017"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "300MG",
        "product_no": "004",
        "approval_date": "Sep 8, 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": "ANDA206923",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Trazodone Hydrochloride",
  "start_marketing_date": "20181005",
  "active_numerator_strength": "50"
}

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