Package 50090-4729-0

{"route": ["ORAL"], "spl_id": "44f75da3-1fee-4928-b8eb-491d47d8bc08", "openfda": {"unii": ["0VE05JYS2P"], "rxcui": ["828348"], "spl_set_id": ["d64ca498-81c6-4e10-ba82-3a50ee47bcfc"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "3 TABLET, FILM COATED in 1 BOTTLE (50090-4729-0)", "package_ndc": "50090-4729-0", "marketing_start_date": "20191118"}, {"sample": false, "description": "12 TABLET, FILM COATED in 1 BOTTLE (50090-4729-1)", "package_ndc": "50090-4729-1", "marketing_start_date": "20191118"}, {"sample": false, "description": "42 TABLET, FILM COATED in 1 BOTTLE (50090-4729-4)", "package_ndc": "50090-4729-4", "marketing_start_date": "20191118"}, {"sample": false, "description": "6 TABLET, FILM COATED in 1 BOTTLE (50090-4729-8)", "package_ndc": "50090-4729-8", "marketing_start_date": "20191118"}], "brand_name": "CYCLOBENZAPRINE HYDROCHLORIDE", "product_id": "50090-4729_44f75da3-1fee-4928-b8eb-491d47d8bc08", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "50090-4729", "generic_name": "cyclobenzaprine hydrochloride", "labeler_name": "A-S Medication Solutions", "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"}