Package 70518-4364-0

{"route": ["ORAL"], "spl_id": "4986f0f6-a218-6af3-e063-6394a90a34d3", "openfda": {"nui": ["N0000175730", "N0000175737"], "unii": ["H0DE420U8G"], "rxcui": ["197502"], "spl_set_id": ["3f73a1d1-b3ee-4678-bc02-3258ec812127"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-4364-0)", "package_ndc": "70518-4364-0", "marketing_start_date": "20250618"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (70518-4364-1)", "package_ndc": "70518-4364-1", "marketing_start_date": "20260129"}], "brand_name": "CHLORZOXAZONE", "product_id": "70518-4364_4986f0f6-a218-6af3-e063-6394a90a34d3", "dosage_form": "TABLET", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "70518-4364", "generic_name": "CHLORZOXAZONE", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CHLORZOXAZONE", "active_ingredients": [{"name": "CHLORZOXAZONE", "strength": "500 mg/1"}], "application_number": "ANDA089853", "marketing_category": "ANDA", "marketing_start_date": "20250618", "listing_expiration_date": "20271231"}