Package 80425-0498-1

{"route": ["ORAL"], "spl_id": "30ca0349-f7a5-388a-e063-6294a90ad02c", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828348"], "spl_set_id": ["30ca08c7-4ee3-2f37-e063-6294a90ae31a"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (80425-0498-1)", "package_ndc": "80425-0498-1", "marketing_start_date": "20250320"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (80425-0498-2)", "package_ndc": "80425-0498-2", "marketing_start_date": "20250320"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (80425-0498-3)", "package_ndc": "80425-0498-3", "marketing_start_date": "20250320"}], "brand_name": "CYCLOBENZAPRINE HYDROCHLORIDE", "product_id": "80425-0498_30ca0349-f7a5-388a-e063-6294a90ad02c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "80425-0498", "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": "ANDA208170", "marketing_category": "ANDA", "marketing_start_date": "20250320", "listing_expiration_date": "20261231"}