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United States · US · US:80425-0276_2a9bad62-b301-697c-e063-6294a90aa395

Tramadol Hydrochloride

Orange BookUNIISPLATC N02AX02

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

Identification

ManufacturerAdvanced Rx Pharmacy of Tennessee, LLC
CountryUS (United States)
ATC codeN02AX02
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 8

  • ndc11
    8042502761
    15 TABLET, COATED in 1 BOTTLE (80425-0276-1)
  • ndc11
    8042502762
    30 TABLET, COATED in 1 BOTTLE (80425-0276-2)
  • ndc11
    8042502763
    60 TABLET, COATED in 1 BOTTLE (80425-0276-3)
  • ndc11
    8042502764
    90 TABLET, COATED in 1 BOTTLE (80425-0276-4)
  • ndc11
    8042502765
    120 TABLET, COATED in 1 BOTTLE (80425-0276-5)
  • ndc11
    8042502766
    40 TABLET, COATED in 1 BOTTLE (80425-0276-6)
  • ndc11
    8042502767
    180 TABLET, COATED in 1 BOTTLE (80425-0276-7)
  • ndc11
    8042502768
    240 TABLET, COATED in 1 BOTTLE (80425-0276-8)

Annotations

UNII (FDA Substance ID)
9N7R477WCK
TRAMADOL HYDROCHLORIDE
RxCUI 82110
Orange Book
A208708
ABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "9N7R477WCK",
    "rxcui": "82110",
    "inchikey": "PPKXEPBICJTCRU-XMZRARIVSA-N;PPKXEPBICJTCRU-KUARMEPBSA-N",
    "display_name": "TRAMADOL HYDROCHLORIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "a6cbd5de-8ae5-49e3-b89b-e35536b115d8": {
      "match": "brand_token",
      "title": "TRAMADOL HYDROCHLORIDE TABLET [STRIDES PHARMA SCIENCE LIMITED]",
      "spl_version": "2",
      "published_date": "2026-06-02"
    }
  },
  "productid": "80425-0276_2a9bad62-b301-697c-e063-6294a90aa395",
  "productndc": "80425-0276",
  "dosage_form": "TABLET, COATED",
  "orange_book": {
    "appl_no": "208708",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "50MG",
        "product_no": "001",
        "approval_date": "Jun 28, 2019"
      },
      {
        "rs": true,
        "rld": false,
        "te_code": "AB",
        "strength": "100MG",
        "product_no": "002",
        "approval_date": "Jun 28, 2019"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "25MG",
        "product_no": "003",
        "approval_date": "Nov 27, 2023"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "75MG",
        "product_no": "004",
        "approval_date": "Apr 4, 2024"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": "CIV",
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "TRAMADOL HYDROCHLORIDE",
  "proprietary_name": "Tramadol Hydrochloride",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA208708",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Tramadol Hydrochloride",
  "start_marketing_date": "20230217",
  "active_numerator_strength": "50"
}

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