Package 72162-2136-9

{"route": ["ORAL"], "spl_id": "b2bf94c3-a8fe-492e-89c4-a4cdb92001a6", "openfda": {"unii": ["3O2T2PJ89D"], "rxcui": ["997229"], "spl_set_id": ["385d2fb5-814c-44bd-ac7b-8857d18f144b"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (72162-2136-0)", "package_ndc": "72162-2136-0", "marketing_start_date": "20210629"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (72162-2136-3)", "package_ndc": "72162-2136-3", "marketing_start_date": "20210629"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (72162-2136-5)", "package_ndc": "72162-2136-5", "marketing_start_date": "20210629"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (72162-2136-9)", "package_ndc": "72162-2136-9", "marketing_start_date": "20210629"}], "brand_name": "Donepezil Hydrochloride", "product_id": "72162-2136_b2bf94c3-a8fe-492e-89c4-a4cdb92001a6", "dosage_form": "TABLET", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "72162-2136", "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": "ANDA078662", "marketing_category": "ANDA", "marketing_start_date": "20210629", "listing_expiration_date": "20261231"}