Package 76420-829-12

{"route": ["ORAL"], "spl_id": "2d48e425-7718-63fa-e063-6394a90ab107", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828299", "828320", "828348"], "spl_set_id": ["418e3974-f7dd-4f27-bee5-3c2fb0531c4c"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (76420-829-01)", "package_ndc": "76420-829-01", "marketing_start_date": "20240702"}, {"sample": false, "description": "7 TABLET, FILM COATED in 1 BOTTLE (76420-829-07)", "package_ndc": "76420-829-07", "marketing_start_date": "20250204"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (76420-829-12)", "package_ndc": "76420-829-12", "marketing_start_date": "20240702"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (76420-829-30)", "package_ndc": "76420-829-30", "marketing_start_date": "20240702"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (76420-829-60)", "package_ndc": "76420-829-60", "marketing_start_date": "20240702"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (76420-829-90)", "package_ndc": "76420-829-90", "marketing_start_date": "20240702"}], "brand_name": "CYCLOBENZAPRINE HYDROCHLORIDE", "product_id": "76420-829_2d48e425-7718-63fa-e063-6394a90ab107", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "76420-829", "generic_name": "cyclobenzaprine hydrochloride", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "CYCLOBENZAPRINE HYDROCHLORIDE", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "7.5 mg/1"}], "application_number": "ANDA208170", "marketing_category": "ANDA", "marketing_start_date": "20170531", "listing_expiration_date": "20261231"}