Package 68071-2999-9
Brand: finasteride
Generic: finasteridePackage Facts
Identity
Package NDC
68071-2999-9
Digits Only
6807129999
Product NDC
68071-2999
Description
90 TABLET, FILM COATED in 1 BOTTLE (68071-2999-9)
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": "2d53f0d0-c914-0b79-e063-6294a90a6bb6", "openfda": {"nui": ["N0000175836", "N0000000126"], "upc": ["0368071299991"], "unii": ["57GNO57U7G"], "rxcui": ["310346"], "spl_set_id": ["fe7e6ea7-583e-22d4-e053-6394a90a2526"], "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": "90 TABLET, FILM COATED in 1 BOTTLE (68071-2999-9)", "package_ndc": "68071-2999-9", "marketing_start_date": "20230619"}], "brand_name": "Finasteride", "product_id": "68071-2999_2d53f0d0-c914-0b79-e063-6294a90a6bb6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["5-alpha Reductase Inhibitor [EPC]", "5-alpha Reductase Inhibitors [MoA]"], "product_ndc": "68071-2999", "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": "ANDA204304", "marketing_category": "ANDA", "marketing_start_date": "20170105", "listing_expiration_date": "20261231"}