Package 71209-020-11

{"route": ["ORAL"], "spl_id": "e33aac76-604d-43cb-8be4-d58ce3b2b6f8", "openfda": {"unii": ["3O2T2PJ89D"], "rxcui": ["997223", "997229"], "spl_set_id": ["37aa1285-774a-4714-a4af-4e3fa9fa7f55"], "manufacturer_name": ["Cadila Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71209-020-01)", "package_ndc": "71209-020-01", "marketing_start_date": "20181124"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71209-020-04)", "package_ndc": "71209-020-04", "marketing_start_date": "20181124"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (71209-020-11)", "package_ndc": "71209-020-11", "marketing_start_date": "20181124"}], "brand_name": "DONEPEZIL HYDROCHLORIDE", "product_id": "71209-020_e33aac76-604d-43cb-8be4-d58ce3b2b6f8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "71209-020", "generic_name": "donepezil hydrochloride", "labeler_name": "Cadila Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DONEPEZIL HYDROCHLORIDE", "active_ingredients": [{"name": "DONEPEZIL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA204609", "marketing_category": "ANDA", "marketing_start_date": "20170130", "listing_expiration_date": "20261231"}