Package 16729-089-10

Brand: finasteride

Generic: finasteride
NDC Package

Package Facts

Identity

Package NDC 16729-089-10
Digits Only 1672908910
Product NDC 16729-089
Product ID 16729-089_2397604d-3fd8-2d97-e063-6394a90a0750
Description

30 TABLET, FILM COATED in 1 BOTTLE (16729-089-10)

Marketing

Marketing Status
Marketed Since 2013-11-08
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": "2397604d-3fd8-2d97-e063-6394a90a0750", "openfda": {"nui": ["N0000175836", "N0000000126"], "upc": ["0316729089104"], "unii": ["57GNO57U7G"], "rxcui": ["200172"], "spl_set_id": ["e3728709-e805-4b46-9954-2c433a865987"], "pharm_class_epc": ["5-alpha Reductase Inhibitor [EPC]"], "pharm_class_moa": ["5-alpha Reductase Inhibitors [MoA]"], "manufacturer_name": ["Accord Healthcare, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (16729-089-10)", "package_ndc": "16729-089-10", "marketing_start_date": "20131108"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (16729-089-15)", "package_ndc": "16729-089-15", "marketing_start_date": "20140117"}], "brand_name": "Finasteride", "product_id": "16729-089_2397604d-3fd8-2d97-e063-6394a90a0750", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["5-alpha Reductase Inhibitor [EPC]", "5-alpha Reductase Inhibitors [MoA]"], "product_ndc": "16729-089", "generic_name": "Finasteride", "labeler_name": "Accord Healthcare, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Finasteride", "active_ingredients": [{"name": "FINASTERIDE", "strength": "1 mg/1"}], "application_number": "ANDA091643", "marketing_category": "ANDA", "marketing_start_date": "20131108", "listing_expiration_date": "20261231"}