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United States · US · US:71335-0325_e3045e19-5284-4f12-9fc8-046a1baf004b

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 · 8

  • ndc11
    7133503251
    60 TABLET, FILM COATED in 1 BOTTLE (71335-0325-1)
  • ndc11
    7133503252
    30 TABLET, FILM COATED in 1 BOTTLE (71335-0325-2)
  • ndc11
    7133503253
    90 TABLET, FILM COATED in 1 BOTTLE (71335-0325-3)
  • ndc11
    7133503254
    120 TABLET, FILM COATED in 1 BOTTLE (71335-0325-4)
  • ndc11
    7133503255
    50 TABLET, FILM COATED in 1 BOTTLE (71335-0325-5)
  • ndc11
    7133503256
    14 TABLET, FILM COATED in 1 BOTTLE (71335-0325-6)
  • ndc11
    7133503257
    45 TABLET, FILM COATED in 1 BOTTLE (71335-0325-7)
  • ndc11
    7133503258
    7 TABLET, FILM COATED in 1 BOTTLE (71335-0325-8)

Annotations

UNII (FDA Substance ID)
0H73WJJ391
TOPIRAMATE
RxCUI 38404
Orange Book
A090278
ABABAB
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": "71335-0325_e3045e19-5284-4f12-9fc8-046a1baf004b",
  "productndc": "71335-0325",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "090278",
    "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": null,
        "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": "ANDA090278",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Topiramate",
  "start_marketing_date": "20141215",
  "active_numerator_strength": "100"
}

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