letrozole

Generic: letrozole

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name letrozole
Generic Name letrozole
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

letrozole 2.5 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-1526
Product ID 71335-1526_3071e8cb-7b32-457a-97e5-145d91034a9b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA200161
Listing Expiration 2026-12-31
Marketing Start 2011-06-04

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 713351526
Hyphenated Format 71335-1526

Supplemental Identifiers

RxCUI
200064
UNII
7LKK855W8I
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 letrozole (source: ndc)
Generic Name letrozole (source: ndc)
Application Number ANDA200161 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2.5 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71335-1526-1)
  • 10 TABLET in 1 BOTTLE (71335-1526-2)
  • 90 TABLET in 1 BOTTLE (71335-1526-3)
  • 40 TABLET in 1 BOTTLE (71335-1526-4)
source: ndc

Packages (4)

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": "3071e8cb-7b32-457a-97e5-145d91034a9b", "openfda": {"nui": ["N0000175563", "N0000175080"], "unii": ["7LKK855W8I"], "rxcui": ["200064"], "spl_set_id": ["3cc750a5-cc88-4b42-b4ab-a87e760f291d"], "pharm_class_epc": ["Aromatase Inhibitor [EPC]"], "pharm_class_moa": ["Aromatase Inhibitors [MoA]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-1526-1)", "package_ndc": "71335-1526-1", "marketing_start_date": "20210201"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (71335-1526-2)", "package_ndc": "71335-1526-2", "marketing_start_date": "20200227"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-1526-3)", "package_ndc": "71335-1526-3", "marketing_start_date": "20221221"}, {"sample": false, "description": "40 TABLET in 1 BOTTLE (71335-1526-4)", "package_ndc": "71335-1526-4", "marketing_start_date": "20210205"}], "brand_name": "LETROZOLE", "product_id": "71335-1526_3071e8cb-7b32-457a-97e5-145d91034a9b", "dosage_form": "TABLET", "pharm_class": ["Aromatase Inhibitor [EPC]", "Aromatase Inhibitors [MoA]"], "product_ndc": "71335-1526", "generic_name": "LETROZOLE", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LETROZOLE", "active_ingredients": [{"name": "LETROZOLE", "strength": "2.5 mg/1"}], "application_number": "ANDA200161", "marketing_category": "ANDA", "marketing_start_date": "20110604", "listing_expiration_date": "20261231"}