Package 62756-194-81

{"route": ["ORAL"], "spl_id": "65890f83-ea1b-4342-b403-6ebe155bc357", "openfda": {"unii": ["3O2T2PJ89D"], "rxcui": ["997223", "997229", "1100184"], "spl_set_id": ["79ad107b-bb20-4ed3-89f0-d7c862f3957c"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (62756-194-18)", "package_ndc": "62756-194-18", "marketing_start_date": "20150617"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (62756-194-81)", "package_ndc": "62756-194-81", "marketing_start_date": "20150617"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (62756-194-83)", "package_ndc": "62756-194-83", "marketing_start_date": "20150617"}], "brand_name": "Donepezil Hydrochloride", "product_id": "62756-194_65890f83-ea1b-4342-b403-6ebe155bc357", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "62756-194", "generic_name": "Donepezil Hydrochloride", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Donepezil Hydrochloride", "active_ingredients": [{"name": "DONEPEZIL HYDROCHLORIDE", "strength": "23 mg/1"}], "application_number": "ANDA204293", "marketing_category": "ANDA", "marketing_start_date": "20150617", "listing_expiration_date": "20261231"}