letrozole

Generic: letrozole tablets

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

Drug Facts

Product Profile

Brand Name letrozole
Generic Name letrozole tablets
Labeler avet pharmaceuticals inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

letrozole 2.5 mg/1

Manufacturer
Avet Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 23155-875
Product ID 23155-875_40009527-770b-8999-e063-6294a90a9946
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205869
Listing Expiration 2026-12-31
Marketing Start 2023-06-01

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 23155875
Hyphenated Format 23155-875

Supplemental Identifiers

RxCUI
200064
UPC
0323155875096 0323155875102 0323155875034
UNII
7LKK855W8I
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 letrozole (source: ndc)
Generic Name letrozole tablets (source: ndc)
Application Number ANDA205869 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2.5 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (23155-875-03)
  • 90 TABLET, FILM COATED in 1 BOTTLE (23155-875-09)
  • 1000 TABLET, FILM COATED in 1 BOTTLE (23155-875-10)
source: ndc

Packages (3)

Ingredients (1)

letrozole (2.5 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "40009527-770b-8999-e063-6294a90a9946", "openfda": {"nui": ["N0000175563", "N0000175080"], "upc": ["0323155875096", "0323155875102", "0323155875034"], "unii": ["7LKK855W8I"], "rxcui": ["200064"], "spl_set_id": ["fe0e4d4b-436d-a36d-e053-6294a90a973d"], "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": true, "description": "30 TABLET, FILM COATED in 1 BOTTLE (23155-875-03)", "package_ndc": "23155-875-03", "marketing_start_date": "20230601"}, {"sample": true, "description": "90 TABLET, FILM COATED in 1 BOTTLE (23155-875-09)", "package_ndc": "23155-875-09", "marketing_start_date": "20230601"}, {"sample": true, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (23155-875-10)", "package_ndc": "23155-875-10", "marketing_start_date": "20230601"}], "brand_name": "Letrozole", "product_id": "23155-875_40009527-770b-8999-e063-6294a90a9946", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Aromatase Inhibitor [EPC]", "Aromatase Inhibitors [MoA]"], "product_ndc": "23155-875", "generic_name": "Letrozole Tablets", "labeler_name": "Avet Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Letrozole", "active_ingredients": [{"name": "LETROZOLE", "strength": "2.5 mg/1"}], "application_number": "ANDA205869", "marketing_category": "ANDA", "marketing_start_date": "20230601", "listing_expiration_date": "20261231"}