Package 50090-4648-0

Brand: finasteride

Generic: finasteride
NDC Package

Package Facts

Identity

Package NDC 50090-4648-0
Digits Only 5009046480
Product NDC 50090-4648
Description

90 TABLET, COATED in 1 BOTTLE (50090-4648-0)

Marketing

Marketing Status
Marketed Since 2019-10-24
Brand finasteride
Generic finasteride
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "01e0d832-7f00-43b6-a131-0cc351bc3ec8", "openfda": {"nui": ["N0000175836", "N0000000126"], "unii": ["57GNO57U7G"], "rxcui": ["200172"], "spl_set_id": ["49eb3a1e-d7e6-4652-aa6d-6abf21af34a6"], "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, COATED in 1 BOTTLE (50090-4648-0)", "package_ndc": "50090-4648-0", "marketing_start_date": "20191024"}], "brand_name": "Finasteride", "product_id": "50090-4648_01e0d832-7f00-43b6-a131-0cc351bc3ec8", "dosage_form": "TABLET, COATED", "pharm_class": ["5-alpha Reductase Inhibitor [EPC]", "5-alpha Reductase Inhibitors [MoA]"], "product_ndc": "50090-4648", "generic_name": "Finasteride", "labeler_name": "A-S Medication Solutions", "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"}