Package 65862-190-05

{"route": ["ORAL"], "spl_id": "13f9bb96-7677-4506-befe-d7afa9b13cab", "openfda": {"upc": ["0365862191014"], "unii": ["0VE05JYS2P"], "rxcui": ["828320", "828348"], "spl_set_id": ["1154688c-1383-442b-a3a5-ec01e038795c"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (65862-190-01)", "package_ndc": "65862-190-01", "marketing_start_date": "20080926"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (65862-190-05)", "package_ndc": "65862-190-05", "marketing_start_date": "20080926"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (65862-190-99)", "package_ndc": "65862-190-99", "marketing_start_date": "20080926"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "65862-190_13f9bb96-7677-4506-befe-d7afa9b13cab", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "65862-190", "generic_name": "Cyclobenzaprine Hydrochloride", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclobenzaprine Hydrochloride", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA078643", "marketing_category": "ANDA", "marketing_start_date": "20080926", "listing_expiration_date": "20261231"}