Package 68071-3475-2

{"route": ["ORAL"], "spl_id": "2bae3004-5267-7ddf-e063-6394a90aa567", "openfda": {"upc": ["0368071347524"], "unii": ["0VE05JYS2P"], "rxcui": ["828320"], "spl_set_id": ["01e18825-1cf9-a98c-e063-6294a90ae0a4"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (68071-3475-1)", "package_ndc": "68071-3475-1", "marketing_start_date": "20230801"}, {"sample": false, "description": "12 TABLET, FILM COATED in 1 BOTTLE (68071-3475-2)", "package_ndc": "68071-3475-2", "marketing_start_date": "20230801"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68071-3475-3)", "package_ndc": "68071-3475-3", "marketing_start_date": "20230801"}, {"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE (68071-3475-4)", "package_ndc": "68071-3475-4", "marketing_start_date": "20240923"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68071-3475-9)", "package_ndc": "68071-3475-9", "marketing_start_date": "20250114"}], "brand_name": "CYCLOBENZAPRINE HYDROCHLORIDE", "product_id": "68071-3475_2bae3004-5267-7ddf-e063-6394a90aa567", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "68071-3475", "generic_name": "cyclobenzaprine hydrochloride", "labeler_name": "NuCare 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": "20170531", "listing_expiration_date": "20261231"}