Package 71335-2093-3

{"route": ["ORAL"], "spl_id": "280c4887-57c3-4d43-afca-98e64de44219", "openfda": {"unii": ["3O2T2PJ89D"], "rxcui": ["997229"], "spl_set_id": ["c030fd7c-da5c-457a-a825-1767bd87d04d"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-2093-1)", "package_ndc": "71335-2093-1", "marketing_start_date": "20240403"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-2093-2)", "package_ndc": "71335-2093-2", "marketing_start_date": "20220506"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-2093-3)", "package_ndc": "71335-2093-3", "marketing_start_date": "20240403"}], "brand_name": "Donepezil Hydrochloride", "product_id": "71335-2093_280c4887-57c3-4d43-afca-98e64de44219", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "71335-2093", "generic_name": "Donepezil Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Donepezil Hydrochloride", "active_ingredients": [{"name": "DONEPEZIL HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA090056", "marketing_category": "ANDA", "marketing_start_date": "20110531", "listing_expiration_date": "20261231"}