Package 80425-0019-2

{"route": ["ORAL"], "spl_id": "2a9878c8-a142-224c-e063-6394a90a839d", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828348"], "spl_set_id": ["afcad582-ab59-4f70-e053-2a95a90a04e4"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (80425-0019-1)", "package_ndc": "80425-0019-1", "marketing_start_date": "20170330"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (80425-0019-2)", "package_ndc": "80425-0019-2", "marketing_start_date": "20170330"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (80425-0019-3)", "package_ndc": "80425-0019-3", "marketing_start_date": "20170330"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "80425-0019_2a9878c8-a142-224c-e063-6394a90a839d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "80425-0019", "generic_name": "Cyclobenzaprine Hydrochloride", "labeler_name": "Advanced Rx of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclobenzaprine Hydrochloride", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA077797", "marketing_category": "ANDA", "marketing_start_date": "20170330", "listing_expiration_date": "20261231"}