Package 70518-3814-3

{"route": ["ORAL"], "spl_id": "43d081b5-edbb-f15e-e063-6394a90a6c2d", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828320"], "spl_set_id": ["5d536e88-62be-45bd-bd09-0efc53fe12b9"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3814-0)", "package_ndc": "70518-3814-0", "marketing_start_date": "20230801"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3814-3)", "package_ndc": "70518-3814-3", "marketing_start_date": "20231007"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3814-5)", "package_ndc": "70518-3814-5", "marketing_start_date": "20231223"}], "brand_name": "CYCLOBENZAPRINE HYDROCHLORIDE", "product_id": "70518-3814_43d081b5-edbb-f15e-e063-6394a90a6c2d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "70518-3814", "generic_name": "cyclobenzaprine hydrochloride", "labeler_name": "REMEDYREPACK 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": "20230801", "listing_expiration_date": "20261231"}