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United States · US · US:71335-1684_97565f5f-1437-4b15-9203-e28fd46d7afc

topiramate

Orange BookUNIISPLATC N03AX11

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

Identification

ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeN03AX11
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 10

  • ndc11
    7133516840
    28 TABLET, FILM COATED in 1 BOTTLE (71335-1684-0)
  • ndc11
    7133516841
    30 TABLET, FILM COATED in 1 BOTTLE (71335-1684-1)
  • ndc11
    7133516842
    60 TABLET, FILM COATED in 1 BOTTLE (71335-1684-2)
  • ndc11
    7133516843
    90 TABLET, FILM COATED in 1 BOTTLE (71335-1684-3)
  • ndc11
    7133516844
    56 TABLET, FILM COATED in 1 BOTTLE (71335-1684-4)
  • ndc11
    7133516845
    84 TABLET, FILM COATED in 1 BOTTLE (71335-1684-5)
  • ndc11
    7133516846
    120 TABLET, FILM COATED in 1 BOTTLE (71335-1684-6)
  • ndc11
    7133516847
    7 TABLET, FILM COATED in 1 BOTTLE (71335-1684-7)
  • ndc11
    7133516848
    14 TABLET, FILM COATED in 1 BOTTLE (71335-1684-8)
  • ndc11
    7133516849
    45 TABLET, FILM COATED in 1 BOTTLE (71335-1684-9)

Annotations

UNII (FDA Substance ID)
0H73WJJ391
TOPIRAMATE
RxCUI 38404
Orange Book
A078235
ABABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "0H73WJJ391",
    "rxcui": "38404",
    "inchikey": "KJADKKWYZYXHBB-XBWDGYHZSA-N",
    "display_name": "TOPIRAMATE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "4e914420-a65b-98ba-e063-6394a90a14c4": {
      "match": "brand_token",
      "title": "TOPIRAMATE SOLUTION [KESIN PHARMA]",
      "spl_version": "1",
      "published_date": "2026-06-01"
    }
  },
  "productid": "71335-1684_97565f5f-1437-4b15-9203-e28fd46d7afc",
  "productndc": "71335-1684",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "078235",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "25MG",
        "product_no": "001",
        "approval_date": "Mar 27, 2009"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "50MG",
        "product_no": "002",
        "approval_date": "Mar 27, 2009"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "100MG",
        "product_no": "003",
        "approval_date": "Mar 27, 2009"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "200MG",
        "product_no": "004",
        "approval_date": "Mar 27, 2009"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "TOPIRAMATE",
  "proprietary_name": "topiramate",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA078235",
  "marketing_category": "ANDA",
  "nonproprietary_name": "topiramate",
  "start_marketing_date": "20090327",
  "active_numerator_strength": "25"
}

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