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United States · US · US:42291-085_485b734b-5e6d-f952-e063-6394a90a3aff

Anastrozole

Orange BookUNIISPLATC L02BG03

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

Identification

ManufacturerAvKARE
CountryUS (United States)
ATC codeL02BG03
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 2

  • ndc11
    4229108530
    30 TABLET, FILM COATED in 1 BOTTLE (42291-085-30)
  • ndc11
    4229108590
    90 TABLET, FILM COATED in 1 BOTTLE (42291-085-90)

Annotations

UNII (FDA Substance ID)
2Z07MYW1AZ
ANASTROZOLE
RxCUI 84857
Orange Book
A078058
AB
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": {
    "513e8413-af48-4acc-e063-6294a90a24b4": {
      "match": "brand_token",
      "title": "ANASTROZOLE (ANASTROZOLE TABLETS) TABLET [NUCARE PHARMACEUTICALS, INC.]",
      "spl_version": "1",
      "published_date": "2026-05-11"
    }
  },
  "productid": "42291-085_485b734b-5e6d-f952-e063-6394a90a3aff",
  "productndc": "42291-085",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "078058",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "1MG",
        "product_no": "001",
        "approval_date": "Jun 28, 2010"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "ANASTROZOLE",
  "proprietary_name": "Anastrozole",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA078058",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Anastrozole",
  "start_marketing_date": "20200313",
  "active_numerator_strength": "1"
}

Related drugs

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