Package 68788-8208-6

{"route": ["ORAL"], "spl_id": "55faf13b-98bb-4ecf-9824-3f9e04c14912", "openfda": {"unii": ["3O2T2PJ89D"], "rxcui": ["997229"], "spl_set_id": ["8138f616-83f3-4c47-84ef-1bce2db339f7"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68788-8208-3)", "package_ndc": "68788-8208-3", "marketing_start_date": "20220603"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68788-8208-6)", "package_ndc": "68788-8208-6", "marketing_start_date": "20220603"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68788-8208-9)", "package_ndc": "68788-8208-9", "marketing_start_date": "20220603"}], "brand_name": "Donepezil Hydrochloride", "product_id": "68788-8208_55faf13b-98bb-4ecf-9824-3f9e04c14912", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "68788-8208", "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": "ANDA090056", "marketing_category": "ANDA", "marketing_start_date": "20220603", "listing_expiration_date": "20261231"}