Package 82009-061-05

Brand: finasteride

Generic: finasteride
NDC Package

Package Facts

Identity

Package NDC 82009-061-05
Digits Only 8200906105
Product NDC 82009-061
Product ID 82009-061_7e56c5b9-a7be-4413-83f2-38c0f3c688e3
Description

500 TABLET, FILM COATED in 1 BOTTLE (82009-061-05)

Marketing

Marketing Status
Marketed Since 2022-11-21
Brand finasteride
Generic finasteride
Sample Package No

Linked Drug Pages (1)

Finasteride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "7e56c5b9-a7be-4413-83f2-38c0f3c688e3", "openfda": {"nui": ["N0000175836", "N0000000126"], "upc": ["0382009061054"], "unii": ["57GNO57U7G"], "rxcui": ["310346"], "spl_set_id": ["5efc695c-d9fd-4892-a63f-a35cceb8d3c7"], "pharm_class_epc": ["5-alpha Reductase Inhibitor [EPC]"], "pharm_class_moa": ["5-alpha Reductase Inhibitors [MoA]"], "manufacturer_name": ["QUALLENT PHARMACEUTICALS HEALTH LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (82009-061-05)", "package_ndc": "82009-061-05", "marketing_start_date": "20221121"}], "brand_name": "Finasteride", "product_id": "82009-061_7e56c5b9-a7be-4413-83f2-38c0f3c688e3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["5-alpha Reductase Inhibitor [EPC]", "5-alpha Reductase Inhibitors [MoA]"], "product_ndc": "82009-061", "generic_name": "Finasteride", "labeler_name": "QUALLENT PHARMACEUTICALS HEALTH LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Finasteride", "active_ingredients": [{"name": "FINASTERIDE", "strength": "5 mg/1"}], "application_number": "ANDA078341", "marketing_category": "ANDA", "marketing_start_date": "20221121", "listing_expiration_date": "20261231"}