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United States · US · US:47335-533_e080bc94-c122-41f3-8bda-0fb9318f8aa6

TRAMADOL HYDROCHLORIDE

Orange BookUNIISPLATC N02AX02

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

Identification

ManufacturerSun Pharmaceutical Industries, Inc.
CountryUS (United States)
ATC codeN02AX02
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 4

  • ndc11
    4733553308
    100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-533-08)
  • ndc11
    4733553318
    1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-533-18)
  • ndc11
    4733553383
    30 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-533-83)
  • ndc11
    4733553388
    100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-533-88)

Annotations

UNII (FDA Substance ID)
9N7R477WCK
TRAMADOL HYDROCHLORIDE
RxCUI 82110
Orange Book
A091607
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": "47335-533_e080bc94-c122-41f3-8bda-0fb9318f8aa6",
  "productndc": "47335-533",
  "dosage_form": "TABLET, EXTENDED RELEASE",
  "orange_book": {
    "appl_no": "091607",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "100MG",
        "product_no": "001",
        "approval_date": "Dec 30, 2011"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "200MG",
        "product_no": "002",
        "approval_date": "Dec 30, 2011"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "300MG",
        "product_no": "003",
        "approval_date": "Dec 30, 2011"
      }
    ],
    "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": "ANDA091607",
  "marketing_category": "ANDA",
  "nonproprietary_name": "TRAMADOL HYDROCHLORIDE",
  "start_marketing_date": "20111230",
  "active_numerator_strength": "200"
}

Related drugs

Other records sharing ATC code N02AX02.

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