Package 68071-3744-6
Brand: finasteride
Generic: finasteridePackage Facts
Identity
Package NDC
68071-3744-6
Digits Only
6807137446
Product NDC
68071-3744
Description
60 TABLET, COATED in 1 BOTTLE (68071-3744-6)
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": "2a091864-3ec9-044f-e063-6294a90adc98", "openfda": {"nui": ["N0000175836", "N0000000126"], "upc": ["0368071374469"], "unii": ["57GNO57U7G"], "rxcui": ["200172"], "spl_set_id": ["291a2037-2b4f-a2fe-e063-6294a90a1e9a"], "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": "60 TABLET, COATED in 1 BOTTLE (68071-3744-6)", "package_ndc": "68071-3744-6", "marketing_start_date": "20241212"}], "brand_name": "Finasteride", "product_id": "68071-3744_2a091864-3ec9-044f-e063-6294a90adc98", "dosage_form": "TABLET, COATED", "pharm_class": ["5-alpha Reductase Inhibitor [EPC]", "5-alpha Reductase Inhibitors [MoA]"], "product_ndc": "68071-3744", "generic_name": "Finasteride", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Finasteride", "active_ingredients": [{"name": "FINASTERIDE", "strength": "1 mg/1"}], "application_number": "ANDA207750", "marketing_category": "ANDA", "marketing_start_date": "20170106", "listing_expiration_date": "20261231"}