ARIMIDEX

Orange BookUNIISPLATC L02BG03

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

Identification

ManufacturerANI Pharmaceuticals, Inc.

CountryUS (United States)

ATC codeL02BG03

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
6255967030
30 TABLET in 1 BOTTLE (62559-670-30)

Annotations

UNII (FDA Substance ID)

2Z07MYW1AZ

ANASTROZOLE

RxCUI 84857

Orange Book

N020541

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "2Z07MYW1AZ",
    "rxcui": "84857",
    "inchikey": "YBBLVLTVTVSKRW-UHFFFAOYSA-N",
    "display_name": "ANASTROZOLE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "acbfaaa9-503c-4691-9828-76a7146ed6de": {
      "match": "brand_token",
      "title": "ARIMIDEX (ANASTROZOLE) TABLET [ANI PHARMACEUTICALS, INC.]",
      "spl_version": "12",
      "published_date": "2026-03-05"
    }
  },
  "productid": "62559-670_e8849657-0444-4ca8-bf66-2017f60d5652",
  "productndc": "62559-670",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "020541",
    "products": [
      {
        "rs": true,
        "rld": true,
        "te_code": "AB",
        "strength": "1MG",
        "product_no": "001",
        "approval_date": "Dec 27, 1995"
      }
    ],
    "appl_type": "N"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "ANASTROZOLE",
  "proprietary_name": "ARIMIDEX",
  "active_ingred_unit": "mg/1",
  "application_number": "NDA020541",
  "marketing_category": "NDA",
  "nonproprietary_name": "Anastrozole",
  "start_marketing_date": "20180626",
  "active_numerator_strength": "1"
}

Related drugs

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