Package 68788-8471-2

{"route": ["ORAL"], "spl_id": "1d5488c5-83a7-4ac9-a55a-b7c87538eeff", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828320"], "spl_set_id": ["e4e8bab3-c5e7-4d2b-9692-ee6c6799b120"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (68788-8471-2)", "package_ndc": "68788-8471-2", "marketing_start_date": "20230629"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68788-8471-3)", "package_ndc": "68788-8471-3", "marketing_start_date": "20230629"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68788-8471-6)", "package_ndc": "68788-8471-6", "marketing_start_date": "20230629"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (68788-8471-8)", "package_ndc": "68788-8471-8", "marketing_start_date": "20230629"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68788-8471-9)", "package_ndc": "68788-8471-9", "marketing_start_date": "20230629"}], "brand_name": "CYCLOBENZAPRINE HYDROCHLORIDE", "product_id": "68788-8471_1d5488c5-83a7-4ac9-a55a-b7c87538eeff", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "68788-8471", "generic_name": "cyclobenzaprine hydrochloride", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CYCLOBENZAPRINE HYDROCHLORIDE", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA208170", "marketing_category": "ANDA", "marketing_start_date": "20230629", "listing_expiration_date": "20261231"}