Package 71335-0900-2

{"route": ["ORAL"], "spl_id": "fde8f515-e602-4b77-a4ad-2e829bdaf193", "openfda": {"unii": ["3O2T2PJ89D"], "rxcui": ["997223"], "spl_set_id": ["c26d9bf3-e148-48bb-8f4f-e8c73804b311"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-0900-1)", "package_ndc": "71335-0900-1", "marketing_start_date": "20191001"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-0900-2)", "package_ndc": "71335-0900-2", "marketing_start_date": "20220128"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-0900-3)", "package_ndc": "71335-0900-3", "marketing_start_date": "20180712"}], "brand_name": "donepezil hydrochloride", "product_id": "71335-0900_fde8f515-e602-4b77-a4ad-2e829bdaf193", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "71335-0900", "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": "10 mg/1"}], "application_number": "ANDA200292", "marketing_category": "ANDA", "marketing_start_date": "20111101", "listing_expiration_date": "20261231"}