Topiramate

Orange BookUNIISPLATC N03AX11

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

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
7133504870
20 TABLET, FILM COATED in 1 BOTTLE (71335-0487-0)
ndc11
7133504871
30 TABLET, FILM COATED in 1 BOTTLE (71335-0487-1)
ndc11
7133504872
60 TABLET, FILM COATED in 1 BOTTLE (71335-0487-2)
ndc11
7133504873
90 TABLET, FILM COATED in 1 BOTTLE (71335-0487-3)
ndc11
7133504874
120 TABLET, FILM COATED in 1 BOTTLE (71335-0487-4)
ndc11
7133504875
7 TABLET, FILM COATED in 1 BOTTLE (71335-0487-5)
ndc11
7133504876
80 TABLET, FILM COATED in 1 BOTTLE (71335-0487-6)
ndc11
7133504877
14 TABLET, FILM COATED in 1 BOTTLE (71335-0487-7)
ndc11
7133504878
45 TABLET, FILM COATED in 1 BOTTLE (71335-0487-8)
ndc11
7133504879
28 TABLET, FILM COATED in 1 BOTTLE (71335-0487-9)

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": "71335-0487_ebf813da-167b-44ed-921d-015fdc8b6d61",
  "productndc": "71335-0487",
  "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": "50"
}

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