Package 16571-779-03

{"route": ["ORAL"], "spl_id": "b963d4b7-66f3-47d7-8671-7412d49e6cb3", "openfda": {"upc": ["0316571778034", "0316571779031"], "unii": ["3O2T2PJ89D"], "rxcui": ["997223", "997229"], "spl_set_id": ["86b0c5a0-ff3c-4840-a4ac-82af922d58bf"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (16571-779-03)", "package_ndc": "16571-779-03", "marketing_start_date": "20110531"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (16571-779-09)", "package_ndc": "16571-779-09", "marketing_start_date": "20110531"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (16571-779-10)", "package_ndc": "16571-779-10", "marketing_start_date": "20110531"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (16571-779-50)", "package_ndc": "16571-779-50", "marketing_start_date": "20110531"}], "brand_name": "Donepezil Hydrochloride", "product_id": "16571-779_b963d4b7-66f3-47d7-8671-7412d49e6cb3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "16571-779", "generic_name": "Donepezil Hydrochloride", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Donepezil Hydrochloride", "active_ingredients": [{"name": "DONEPEZIL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA090056", "marketing_category": "ANDA", "marketing_start_date": "20110531", "listing_expiration_date": "20261231"}