Package 85509-1014-3

{"route": ["ORAL"], "spl_id": "3a90172c-fe2c-0eee-e063-6294a90a6018", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828348"], "spl_set_id": ["3a90171b-aef3-0691-e063-6294a90a6560"], "manufacturer_name": ["PHOENIX RX LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (85509-1014-3)", "package_ndc": "85509-1014-3", "marketing_start_date": "20250722"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (85509-1014-6)", "package_ndc": "85509-1014-6", "marketing_start_date": "20250722"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (85509-1014-9)", "package_ndc": "85509-1014-9", "marketing_start_date": "20250722"}], "brand_name": "CYCLOBENZAPRINE HYDROCHLORIDE", "product_id": "85509-1014_3a90172c-fe2c-0eee-e063-6294a90a6018", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "85509-1014", "generic_name": "cyclobenzaprine hydrochloride", "labeler_name": "PHOENIX RX LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CYCLOBENZAPRINE HYDROCHLORIDE", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA208170", "marketing_category": "ANDA", "marketing_start_date": "20250320", "listing_expiration_date": "20261231"}