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United States · US · US:62756-259_d0c9002b-fa32-4ca8-862f-5286746df2cb

Zonisamide

Orange BookUNIISPLATC N03AX15

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

Identification

ManufacturerSun Pharmaceutical Industries, Inc.
CountryUS (United States)
ATC codeN03AX15
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 4

  • ndc11
    6275625901
    30 CAPSULE in 1 BOTTLE (62756-259-01)
  • ndc11
    6275625902
    100 CAPSULE in 1 BOTTLE (62756-259-02)
  • ndc11
    6275625903
    100 CAPSULE in 1 BOTTLE (62756-259-03)
  • ndc11
    6275625904
    1000 CAPSULE in 1 BOTTLE (62756-259-04)

Annotations

UNII (FDA Substance ID)
459384H98V
ZONISAMIDE
RxCUI 39998
Orange Book
A077634
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "459384H98V",
    "rxcui": "39998",
    "inchikey": "UBQNRHZMVUUOMG-UHFFFAOYSA-N",
    "display_name": "ZONISAMIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "50bb1a0a-a66d-4a13-a456-a10c1b8c8e94": {
      "match": "brand_token",
      "title": "ZONISAMIDE CAPSULE [REMEDYREPACK INC.]",
      "spl_version": "2",
      "published_date": "2026-05-28"
    }
  },
  "productid": "62756-259_d0c9002b-fa32-4ca8-862f-5286746df2cb",
  "productndc": "62756-259",
  "dosage_form": "CAPSULE",
  "orange_book": {
    "appl_no": "077634",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "25MG",
        "product_no": "001",
        "approval_date": "Mar 17, 2006"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "50MG",
        "product_no": "002",
        "approval_date": "Mar 17, 2006"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "100MG",
        "product_no": "003",
        "approval_date": "Mar 17, 2006"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "ZONISAMIDE",
  "proprietary_name": "Zonisamide",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA077634",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Zonisamide",
  "start_marketing_date": "20060317",
  "active_numerator_strength": "50"
}

Related drugs

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