Package 71093-127-05

{"route": ["ORAL"], "spl_id": "a4736add-da84-411f-8e6f-9de67bf467f8", "openfda": {"unii": ["3O2T2PJ89D"], "rxcui": ["997223", "997229"], "spl_set_id": ["297e86e8-d248-4cc9-9d9c-2ef9efb4414d"], "manufacturer_name": ["ACI Healthcare USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71093-127-01)", "package_ndc": "71093-127-01", "marketing_start_date": "20210629"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71093-127-03)", "package_ndc": "71093-127-03", "marketing_start_date": "20210629"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (71093-127-05)", "package_ndc": "71093-127-05", "marketing_start_date": "20210629"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (71093-127-06)", "package_ndc": "71093-127-06", "marketing_start_date": "20210629"}], "brand_name": "Donepezil Hydrochloride", "product_id": "71093-127_a4736add-da84-411f-8e6f-9de67bf467f8", "dosage_form": "TABLET", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "71093-127", "generic_name": "Donepezil Hydrochloride", "labeler_name": "ACI Healthcare USA, Inc.", "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"}