Package 71335-0433-3
Brand: finasteride
Generic: finasteridePackage Facts
Identity
Package NDC
71335-0433-3
Digits Only
7133504333
Product NDC
71335-0433
Description
60 TABLET, FILM COATED in 1 BOTTLE (71335-0433-3)
Marketing
Marketing Status
Brand
finasteride
Generic
finasteride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "965d1a37-d574-4894-b08e-c6f21b882379", "openfda": {"nui": ["N0000175836", "N0000000126"], "unii": ["57GNO57U7G"], "rxcui": ["310346"], "spl_set_id": ["ef9c0b23-4736-4fb0-862c-c2a4d644e0d6"], "pharm_class_epc": ["5-alpha Reductase Inhibitor [EPC]"], "pharm_class_moa": ["5-alpha Reductase Inhibitors [MoA]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (71335-0433-1)", "package_ndc": "71335-0433-1", "marketing_start_date": "20211216"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-0433-2)", "package_ndc": "71335-0433-2", "marketing_start_date": "20180314"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-0433-3)", "package_ndc": "71335-0433-3", "marketing_start_date": "20210127"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-0433-4)", "package_ndc": "71335-0433-4", "marketing_start_date": "20180503"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (71335-0433-5)", "package_ndc": "71335-0433-5", "marketing_start_date": "20180521"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (71335-0433-6)", "package_ndc": "71335-0433-6", "marketing_start_date": "20241030"}], "brand_name": "Finasteride", "product_id": "71335-0433_965d1a37-d574-4894-b08e-c6f21b882379", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["5-alpha Reductase Inhibitor [EPC]", "5-alpha Reductase Inhibitors [MoA]"], "product_ndc": "71335-0433", "generic_name": "finasteride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Finasteride", "active_ingredients": [{"name": "FINASTERIDE", "strength": "5 mg/1"}], "application_number": "ANDA090121", "marketing_category": "ANDA", "marketing_start_date": "20100528", "listing_expiration_date": "20261231"}