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United States · US · US:70771-1374_7892e262-ddad-4e1d-909d-d8590bb082de

Exemestane

Orange BookUNIISPLATC L02BG06

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

Identification

ManufacturerZydus Lifesciences Limited
CountryUS (United States)
ATC codeL02BG06
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    7077113743
    30 TABLET in 1 BOTTLE (70771-1374-3)

Annotations

UNII (FDA Substance ID)
NY22HMQ4BX
EXEMESTANE
RxCUI 258494
Orange Book
A202602
AB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "NY22HMQ4BX",
    "rxcui": "258494",
    "inchikey": "BFYIZQONLCFLEV-DAELLWKTSA-N",
    "display_name": "EXEMESTANE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "69abd0ff-b200-4d1a-b14a-80e980a8e781": {
      "match": "brand_token",
      "title": "EXEMESTANE TABLET, SUGAR COATED [MYLAN PHARMACEUTICALS INC.]",
      "spl_version": "20",
      "published_date": "2025-12-25"
    }
  },
  "productid": "70771-1374_7892e262-ddad-4e1d-909d-d8590bb082de",
  "productndc": "70771-1374",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "202602",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "25MG",
        "product_no": "001",
        "approval_date": "Oct 3, 2018"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "EXEMESTANE",
  "proprietary_name": "Exemestane",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA202602",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Exemestane",
  "start_marketing_date": "20181008",
  "active_numerator_strength": "25"
}

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