anastrozole

Generic: anastrozole

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name anastrozole
Generic Name anastrozole
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

anastrozole 1 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-342
Product ID 72789-342_2e80f27e-47c5-0ddc-e063-6294a90a089c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078921
Listing Expiration 2026-12-31
Marketing Start 2010-06-27

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 72789342
Hyphenated Format 72789-342

Supplemental Identifiers

RxCUI
199224
UPC
0372789342153
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 ANDA078921 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 15 TABLET, COATED in 1 BOTTLE, PLASTIC (72789-342-15)
source: ndc

Packages (1)

Ingredients (1)

anastrozole (1 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2e80f27e-47c5-0ddc-e063-6294a90a089c", "openfda": {"nui": ["N0000175563", "N0000175080"], "upc": ["0372789342153"], "unii": ["2Z07MYW1AZ"], "rxcui": ["199224"], "spl_set_id": ["b023a9f2-1a99-4b40-a953-edac7e3a79bf"], "pharm_class_epc": ["Aromatase Inhibitor [EPC]"], "pharm_class_moa": ["Aromatase Inhibitors [MoA]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET, COATED in 1 BOTTLE, PLASTIC (72789-342-15)", "package_ndc": "72789-342-15", "marketing_start_date": "20230901"}], "brand_name": "Anastrozole", "product_id": "72789-342_2e80f27e-47c5-0ddc-e063-6294a90a089c", "dosage_form": "TABLET, COATED", "pharm_class": ["Aromatase Inhibitor [EPC]", "Aromatase Inhibitors [MoA]"], "product_ndc": "72789-342", "generic_name": "Anastrozole", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Anastrozole", "active_ingredients": [{"name": "ANASTROZOLE", "strength": "1 mg/1"}], "application_number": "ANDA078921", "marketing_category": "ANDA", "marketing_start_date": "20100627", "listing_expiration_date": "20261231"}