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United States · US · US:70518-1718_50ae93f2-7103-297d-e063-6294a90a141e

topiramate

Orange BookUNIISPLATC N03AX11

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

Identification

ManufacturerREMEDYREPACK INC.
CountryUS (United States)
ATC codeN03AX11
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 4

  • ndc11
    7051817180
    30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1718-0)
  • ndc11
    7051817181
    30 POUCH in 1 BOX (70518-1718-1) / 1 TABLET, FILM COATED in 1 POUCH (70518-1718-2)
  • ndc11
    7051817183
    90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1718-3)
  • ndc11
    7051817184
    60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1718-4)

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": "70518-1718_50ae93f2-7103-297d-e063-6294a90a141e",
  "productndc": "70518-1718",
  "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": "20181207",
  "active_numerator_strength": "25"
}

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