Package 0615-8313-30

{"route": ["ORAL"], "spl_id": "d950c91f-51cd-4f96-8562-971798db2edf", "openfda": {"unii": ["3O2T2PJ89D"], "rxcui": ["997223"], "spl_set_id": ["7620f41a-3eef-453b-a564-ea3c85374de2"], "manufacturer_name": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET, FILM COATED in 1 BLISTER PACK (0615-8313-05)", "package_ndc": "0615-8313-05", "marketing_start_date": "20190821"}, {"sample": false, "description": "28 TABLET, FILM COATED in 1 BLISTER PACK (0615-8313-28)", "package_ndc": "0615-8313-28", "marketing_start_date": "20250106"}, {"sample": false, "description": "6 BLISTER PACK in 1 BOX, UNIT-DOSE (0615-8313-30)  / 5 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0615-8313-30", "marketing_start_date": "20190819"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8313-39)", "package_ndc": "0615-8313-39", "marketing_start_date": "20190821"}], "brand_name": "Donepezil Hydrochloride", "product_id": "0615-8313_d950c91f-51cd-4f96-8562-971798db2edf", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "0615-8313", "generic_name": "Donepezil Hydrochloride", "labeler_name": "NCS HealthCare of KY, LLC dba Vangard Labs", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Donepezil Hydrochloride", "active_ingredients": [{"name": "DONEPEZIL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA201146", "marketing_category": "ANDA", "marketing_start_date": "20120817", "listing_expiration_date": "20261231"}