Package 62332-092-90

{"route": ["ORAL"], "spl_id": "cd86384e-917a-41f3-9d71-900c45d83651", "openfda": {"unii": ["3O2T2PJ89D"], "rxcui": ["997223", "997229"], "spl_set_id": ["9407258b-60ed-4884-a903-885aeedaddf8"], "manufacturer_name": ["Alembic Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 CARTON (62332-092-10)", "package_ndc": "62332-092-10", "marketing_start_date": "20160129"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (62332-092-30)", "package_ndc": "62332-092-30", "marketing_start_date": "20160129"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (62332-092-90)", "package_ndc": "62332-092-90", "marketing_start_date": "20160129"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (62332-092-91)", "package_ndc": "62332-092-91", "marketing_start_date": "20160129"}], "brand_name": "Donepezil Hydrochloride", "product_id": "62332-092_cd86384e-917a-41f3-9d71-900c45d83651", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "62332-092", "generic_name": "Donepezil Hydrochloride", "labeler_name": "Alembic Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Donepezil Hydrochloride", "active_ingredients": [{"name": "DONEPEZIL HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA201724", "marketing_category": "ANDA", "marketing_start_date": "20160129", "listing_expiration_date": "20261231"}