Package 85509-1415-3

{"route": ["ORAL"], "spl_id": "4383b050-63c1-5a35-e063-6294a90a8a05", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828348"], "spl_set_id": ["4383b26f-c39f-3d6a-e063-6294a90aba03"], "manufacturer_name": ["PHOENIX RX LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (85509-1415-3)", "package_ndc": "85509-1415-3", "marketing_start_date": "20251114"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (85509-1415-6)", "package_ndc": "85509-1415-6", "marketing_start_date": "20251114"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (85509-1415-9)", "package_ndc": "85509-1415-9", "marketing_start_date": "20251114"}], "brand_name": "Cyclobenzaprine hydrochloride", "product_id": "85509-1415_4383b050-63c1-5a35-e063-6294a90a8a05", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "85509-1415", "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": "ANDA213324", "marketing_category": "ANDA", "marketing_start_date": "20200706", "listing_expiration_date": "20261231"}