anastrozole

Generic: anastrozole tablets

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name anastrozole
Generic Name anastrozole tablets
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

anastrozole 1 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 82804-162
Product ID 82804-162_db39f10e-5444-4e57-97b2-0358001df04a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206037
Listing Expiration 2026-12-31
Marketing Start 2019-02-28

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 82804162
Hyphenated Format 82804-162

Supplemental Identifiers

RxCUI
199224
UPC
0382804162307
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 tablets (source: ndc)
Application Number ANDA206037 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (82804-162-30)
  • 90 TABLET in 1 BOTTLE (82804-162-90)
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": "db39f10e-5444-4e57-97b2-0358001df04a", "openfda": {"nui": ["N0000175563", "N0000175080"], "upc": ["0382804162307"], "unii": ["2Z07MYW1AZ"], "rxcui": ["199224"], "spl_set_id": ["2df2aa01-1fe7-477c-9a23-699879b0b918"], "pharm_class_epc": ["Aromatase Inhibitor [EPC]"], "pharm_class_moa": ["Aromatase Inhibitors [MoA]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (82804-162-30)", "package_ndc": "82804-162-30", "marketing_start_date": "20241025"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (82804-162-90)", "package_ndc": "82804-162-90", "marketing_start_date": "20250916"}], "brand_name": "Anastrozole", "product_id": "82804-162_db39f10e-5444-4e57-97b2-0358001df04a", "dosage_form": "TABLET", "pharm_class": ["Aromatase Inhibitor [EPC]", "Aromatase Inhibitors [MoA]"], "product_ndc": "82804-162", "generic_name": "Anastrozole Tablets", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Anastrozole", "active_ingredients": [{"name": "ANASTROZOLE", "strength": "1 mg/1"}], "application_number": "ANDA206037", "marketing_category": "ANDA", "marketing_start_date": "20190228", "listing_expiration_date": "20261231"}