anastrozole

Generic: anastrozole

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name anastrozole
Generic Name anastrozole
Labeler direct_rx
Dosage Form TABLET
Routes
ORAL
Active Ingredients

anastrozole 1 mg/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 72189-415
Product ID 72189-415_2c4d028d-1373-45ab-e063-6394a90a0353
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090568
Listing Expiration 2026-12-31
Marketing Start 2023-01-30

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 72189415
Hyphenated Format 72189-415

Supplemental Identifiers

RxCUI
199224
UNII
2Z07MYW1AZ
NUI
N0000175563 N0000175080

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 ANDA090568 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (72189-415-30)
source: ndc

Packages (1)

72189-415-30 30 TABLET in 1 BOTTLE (72189-415-30)

Ingredients (1)

anastrozole (1 mg/1)

Linked Drug Pages (1)

ANASTROZOLE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2c4d028d-1373-45ab-e063-6394a90a0353", "openfda": {"nui": ["N0000175563", "N0000175080"], "unii": ["2Z07MYW1AZ"], "rxcui": ["199224"], "spl_set_id": ["f37db328-bb81-9df9-e053-2a95a90a6f43"], "pharm_class_epc": ["Aromatase Inhibitor [EPC]"], "pharm_class_moa": ["Aromatase Inhibitors [MoA]"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-415-30)", "package_ndc": "72189-415-30", "marketing_start_date": "20230130"}], "brand_name": "ANASTROZOLE", "product_id": "72189-415_2c4d028d-1373-45ab-e063-6394a90a0353", "dosage_form": "TABLET", "pharm_class": ["Aromatase Inhibitor [EPC]", "Aromatase Inhibitors [MoA]"], "product_ndc": "72189-415", "generic_name": "ANASTROZOLE", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ANASTROZOLE", "active_ingredients": [{"name": "ANASTROZOLE", "strength": "1 mg/1"}], "application_number": "ANDA090568", "marketing_category": "ANDA", "marketing_start_date": "20230130", "listing_expiration_date": "20261231"}