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United States · US · US:42806-097_e68d74c7-1d6a-4453-bb46-0047047b7527

Protriptyline Hydrochloride

Orange BookUNIISPLATC N06AA11

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

Identification

ManufacturerEpic Pharma, LLC
CountryUS (United States)
ATC codeN06AA11
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 3

  • ndc11
    4280609701
    100 TABLET, FILM COATED in 1 BOTTLE (42806-097-01)
  • ndc11
    4280609710
    1000 TABLET, FILM COATED in 1 BOTTLE (42806-097-10)
  • ndc11
    4280609730
    30 TABLET, FILM COATED in 1 BOTTLE (42806-097-30)

Annotations

UNII (FDA Substance ID)
44665V00O8
PROTRIPTYLINE HYDROCHLORIDE
RxCUI 203199
Orange Book
A202220
ABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "44665V00O8",
    "rxcui": "203199",
    "inchikey": "OGQDIIKRQRZXJH-UHFFFAOYSA-N",
    "display_name": "PROTRIPTYLINE HYDROCHLORIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "c6c7c39e-e510-4f4a-bf7a-926f0e075d3a": {
      "match": "brand_token",
      "title": "PROTRIPTYLINE HYDROCHLORIDE TABLET, FILM COATED [EPIC PHARMA, LLC]",
      "spl_version": "10",
      "published_date": "2023-12-21"
    }
  },
  "productid": "42806-097_e68d74c7-1d6a-4453-bb46-0047047b7527",
  "productndc": "42806-097",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "202220",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "5MG",
        "product_no": "001",
        "approval_date": "Nov 19, 2012"
      },
      {
        "rs": true,
        "rld": false,
        "te_code": "AB",
        "strength": "10MG",
        "product_no": "002",
        "approval_date": "Nov 19, 2012"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "PROTRIPTYLINE HYDROCHLORIDE",
  "proprietary_name": "Protriptyline Hydrochloride",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA202220",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Protriptyline Hydrochloride",
  "start_marketing_date": "20130109",
  "active_numerator_strength": "10"
}

Related drugs

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