anastrozole

Generic: anastrozole tablets

Labeler: avet pharmaceuticals inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name anastrozole
Generic Name anastrozole tablets
Labeler avet pharmaceuticals inc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

anastrozole 1 mg/1

Manufacturer
Avet Pharmaceuticals Inc

Identifiers & Regulatory

Product NDC 23155-857
Product ID 23155-857_4713d319-eace-08c3-e063-6294a90ac02d
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 23155857
Hyphenated Format 23155-857

Supplemental Identifiers

RxCUI
199224
UPC
0323155857092 0323155857030 0323155857054
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 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 (23155-857-03)
  • 500 TABLET in 1 BOTTLE (23155-857-05)
  • 90 TABLET in 1 BOTTLE (23155-857-09)
source: ndc

Packages (3)

Ingredients (1)

anastrozole (1 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4713d319-eace-08c3-e063-6294a90ac02d", "openfda": {"nui": ["N0000175563", "N0000175080"], "upc": ["0323155857092", "0323155857030", "0323155857054"], "unii": ["2Z07MYW1AZ"], "rxcui": ["199224"], "spl_set_id": ["f86d2158-b078-3f74-e053-6394a90aa4b6"], "pharm_class_epc": ["Aromatase Inhibitor [EPC]"], "pharm_class_moa": ["Aromatase Inhibitors [MoA]"], "manufacturer_name": ["Avet Pharmaceuticals Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (23155-857-03)", "package_ndc": "23155-857-03", "marketing_start_date": "20190228"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (23155-857-05)", "package_ndc": "23155-857-05", "marketing_start_date": "20190228"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (23155-857-09)", "package_ndc": "23155-857-09", "marketing_start_date": "20190228"}], "brand_name": "Anastrozole", "product_id": "23155-857_4713d319-eace-08c3-e063-6294a90ac02d", "dosage_form": "TABLET", "pharm_class": ["Aromatase Inhibitor [EPC]", "Aromatase Inhibitors [MoA]"], "product_ndc": "23155-857", "generic_name": "Anastrozole Tablets", "labeler_name": "Avet Pharmaceuticals Inc", "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"}