Anastrozole

Orange BookUNIISPLATC L02BG03

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

Identification

ManufacturerPD-Rx Pharmaceuticals, Inc.

CountryUS (United States)

ATC codeL02BG03

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
7278934215
15 TABLET, COATED in 1 BOTTLE, PLASTIC (72789-342-15)

Annotations

UNII (FDA Substance ID)

2Z07MYW1AZ

ANASTROZOLE

RxCUI 84857

Orange Book

A078921

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": "72789-342_2e80f27e-47c5-0ddc-e063-6294a90a089c",
  "productndc": "72789-342",
  "dosage_form": "TABLET, COATED",
  "orange_book": {
    "appl_no": "078921",
    "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": "ANDA078921",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Anastrozole",
  "start_marketing_date": "20100627",
  "active_numerator_strength": "1"
}

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