Package 68071-3462-5

{"route": ["ORAL"], "spl_id": "14a7402c-8406-3acb-e063-6394a90a6b7f", "openfda": {"upc": ["0368071346220"], "unii": ["0VE05JYS2P"], "rxcui": ["828348"], "spl_set_id": ["00dbe051-a392-e2c6-e063-6394a90ab7f3"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (68071-3462-2)", "package_ndc": "68071-3462-2", "marketing_start_date": "20230719"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68071-3462-3)", "package_ndc": "68071-3462-3", "marketing_start_date": "20230731"}, {"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE (68071-3462-5)", "package_ndc": "68071-3462-5", "marketing_start_date": "20230719"}], "brand_name": "CYCLOBENZAPRINE HYDROCHLORIDE", "product_id": "68071-3462_14a7402c-8406-3acb-e063-6394a90a6b7f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "68071-3462", "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": "10 mg/1"}], "application_number": "ANDA208170", "marketing_category": "ANDA", "marketing_start_date": "20170531", "listing_expiration_date": "20261231"}