Package 68071-3785-2
Brand: finasteride
Generic: finasteridePackage Facts
Identity
Package NDC
68071-3785-2
Digits Only
6807137852
Product NDC
68071-3785
Description
120 TABLET, FILM COATED in 1 BOTTLE (68071-3785-2)
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": "40bd923b-50f8-c9dd-e063-6294a90a71f3", "openfda": {"nui": ["N0000175836", "N0000000126"], "upc": ["0368071378580"], "unii": ["57GNO57U7G"], "rxcui": ["310346"], "spl_set_id": ["2c688ec5-1b0f-2269-e063-6394a90a7220"], "pharm_class_epc": ["5-alpha Reductase Inhibitor [EPC]"], "pharm_class_moa": ["5-alpha Reductase Inhibitors [MoA]"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (68071-3785-2)", "package_ndc": "68071-3785-2", "marketing_start_date": "20250123"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68071-3785-6)", "package_ndc": "68071-3785-6", "marketing_start_date": "20251009"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (68071-3785-8)", "package_ndc": "68071-3785-8", "marketing_start_date": "20250123"}], "brand_name": "Finasteride", "product_id": "68071-3785_40bd923b-50f8-c9dd-e063-6294a90a71f3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["5-alpha Reductase Inhibitor [EPC]", "5-alpha Reductase Inhibitors [MoA]"], "product_ndc": "68071-3785", "generic_name": "Finasteride", "labeler_name": "NuCare Pharmaceuticals, Inc.", "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": "20071030", "listing_expiration_date": "20261231"}