Package 42658-120-08

{"route": ["ORAL"], "spl_id": "2c703e82-e970-a97e-e063-6294a90a1639", "openfda": {"upc": ["0342658120083", "0342658119087", "0342658119513", "0342658120014", "0342658119049", "0342658119018", "0342658120519", "0342658120045"], "unii": ["3O2T2PJ89D"], "rxcui": ["997220", "997226"], "spl_set_id": ["8d682a51-31d0-43e6-9fab-6eb5219f5a41"], "manufacturer_name": ["Hisun Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (42658-120-01)", "package_ndc": "42658-120-01", "marketing_start_date": "20250101"}, {"sample": false, "description": "90 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (42658-120-04)", "package_ndc": "42658-120-04", "marketing_start_date": "20250101"}, {"sample": false, "description": "1000 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (42658-120-08)", "package_ndc": "42658-120-08", "marketing_start_date": "20250101"}, {"sample": false, "description": "3 BLISTER PACK in 1 CARTON (42658-120-51)  / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK", "package_ndc": "42658-120-51", "marketing_start_date": "20250101"}], "brand_name": "Donepezil Hydrochloride", "product_id": "42658-120_2c703e82-e970-a97e-e063-6294a90a1639", "dosage_form": "TABLET, ORALLY DISINTEGRATING", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "42658-120", "generic_name": "donepezil hydrochloride", "labeler_name": "Hisun Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Donepezil Hydrochloride", "active_ingredients": [{"name": "DONEPEZIL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA205269", "marketing_category": "ANDA", "marketing_start_date": "20250101", "listing_expiration_date": "20261231"}