anastrozole

Generic: anastrozole

Labeler: aurobindo pharma limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name anastrozole
Generic Name anastrozole
Labeler aurobindo pharma limited
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

anastrozole 1 mg/1

Manufacturer
Aurobindo Pharma Limited

Identifiers & Regulatory

Product NDC 59651-236
Product ID 59651-236_6b709b22-b3d8-4846-b48e-b975a80c0998
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212434
Listing Expiration 2026-12-31
Marketing Start 2020-07-24

Pharmacologic Class

Established (EPC)
aromatase inhibitor [epc]
Mechanism of Action
aromatase inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 59651236
Hyphenated Format 59651-236

Supplemental Identifiers

RxCUI
199224
UPC
0359651236901 0359651236307
UNII
2Z07MYW1AZ
NUI
N0000175563 N0000175080

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name anastrozole (source: ndc)
Generic Name anastrozole (source: ndc)
Application Number ANDA212434 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (59651-236-30)
  • 90 TABLET, FILM COATED in 1 BOTTLE (59651-236-90)
source: ndc

Packages (2)

Ingredients (1)

anastrozole (1 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6b709b22-b3d8-4846-b48e-b975a80c0998", "openfda": {"nui": ["N0000175563", "N0000175080"], "upc": ["0359651236901", "0359651236307"], "unii": ["2Z07MYW1AZ"], "rxcui": ["199224"], "spl_set_id": ["71f053c2-8d0d-41a1-8630-2d797eced799"], "pharm_class_epc": ["Aromatase Inhibitor [EPC]"], "pharm_class_moa": ["Aromatase Inhibitors [MoA]"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (59651-236-30)", "package_ndc": "59651-236-30", "marketing_start_date": "20200724"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (59651-236-90)", "package_ndc": "59651-236-90", "marketing_start_date": "20200724"}], "brand_name": "Anastrozole", "product_id": "59651-236_6b709b22-b3d8-4846-b48e-b975a80c0998", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Aromatase Inhibitor [EPC]", "Aromatase Inhibitors [MoA]"], "product_ndc": "59651-236", "generic_name": "Anastrozole", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Anastrozole", "active_ingredients": [{"name": "ANASTROZOLE", "strength": "1 mg/1"}], "application_number": "ANDA212434", "marketing_category": "ANDA", "marketing_start_date": "20200724", "listing_expiration_date": "20261231"}