Package 50090-7086-0

Brand: finasteride

Generic: finasteride
NDC Package

Package Facts

Identity

Package NDC 50090-7086-0
Digits Only 5009070860
Product NDC 50090-7086
Description

90 TABLET, FILM COATED in 1 BOTTLE (50090-7086-0)

Marketing

Marketing Status
Marketed Since 2024-02-06
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": "507dd7a1-574d-4c9b-a5eb-16b48455e5c3", "openfda": {"nui": ["N0000175836", "N0000000126"], "unii": ["57GNO57U7G"], "rxcui": ["310346"], "spl_set_id": ["e6ee2f07-63a6-4fde-88de-654bf633529e"], "pharm_class_epc": ["5-alpha Reductase Inhibitor [EPC]"], "pharm_class_moa": ["5-alpha Reductase Inhibitors [MoA]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-7086-0)", "package_ndc": "50090-7086-0", "marketing_start_date": "20240206"}], "brand_name": "Finasteride", "product_id": "50090-7086_507dd7a1-574d-4c9b-a5eb-16b48455e5c3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["5-alpha Reductase Inhibitor [EPC]", "5-alpha Reductase Inhibitors [MoA]"], "product_ndc": "50090-7086", "generic_name": "Finasteride", "labeler_name": "A-S Medication Solutions", "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"}