Package 65862-325-01

{"route": ["ORAL"], "spl_id": "3c956648-d46c-41e2-a2d9-8560846a7a32", "openfda": {"unii": ["3O2T2PJ89D"], "rxcui": ["997223", "997229"], "spl_set_id": ["3257494f-8f44-4978-b92d-bde87b2444b6"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (65862-325-01)", "package_ndc": "65862-325-01", "marketing_start_date": "20110531"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (65862-325-05)", "package_ndc": "65862-325-05", "marketing_start_date": "20110531"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (65862-325-10)  / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "65862-325-10", "marketing_start_date": "20110531"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (65862-325-30)", "package_ndc": "65862-325-30", "marketing_start_date": "20110531"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (65862-325-90)", "package_ndc": "65862-325-90", "marketing_start_date": "20110531"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (65862-325-99)", "package_ndc": "65862-325-99", "marketing_start_date": "20110531"}], "brand_name": "Donepezil Hydrochloride", "product_id": "65862-325_3c956648-d46c-41e2-a2d9-8560846a7a32", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "65862-325", "generic_name": "Donepezil Hydrochloride", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Donepezil Hydrochloride", "active_ingredients": [{"name": "DONEPEZIL HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA090056", "marketing_category": "ANDA", "marketing_start_date": "20110531", "listing_expiration_date": "20261231"}