Package 68788-8711-3

{"route": ["ORAL"], "spl_id": "8f19ad1f-55f0-4e87-bb19-4c89f900850d", "openfda": {"unii": ["3O2T2PJ89D"], "rxcui": ["997229"], "spl_set_id": ["ee54a472-6783-41df-b8bb-9c3e4c996907"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-8711-3)", "package_ndc": "68788-8711-3", "marketing_start_date": "20240708"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68788-8711-6)", "package_ndc": "68788-8711-6", "marketing_start_date": "20240708"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-8711-9)", "package_ndc": "68788-8711-9", "marketing_start_date": "20240708"}], "brand_name": "Donepezil Hydrochloride", "product_id": "68788-8711_8f19ad1f-55f0-4e87-bb19-4c89f900850d", "dosage_form": "TABLET", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "68788-8711", "generic_name": "Donepezil Hydrochloride", "labeler_name": "Preferred Pharmaceuticals 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": "20240708", "listing_expiration_date": "20261231"}