Package 65162-541-11

{"route": ["ORAL"], "spl_id": "df260758-80f8-4668-884c-7fb21600db2e", "openfda": {"upc": ["0365162541106", "0365162540109"], "unii": ["0VE05JYS2P"], "rxcui": ["828320", "828348"], "spl_set_id": ["390151d4-5fcb-46e2-92e6-de184827f43d"], "manufacturer_name": ["Amneal Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (65162-541-10)", "package_ndc": "65162-541-10", "marketing_start_date": "20100218"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (65162-541-11)", "package_ndc": "65162-541-11", "marketing_start_date": "20100218"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (65162-541-50)", "package_ndc": "65162-541-50", "marketing_start_date": "20100218"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "65162-541_df260758-80f8-4668-884c-7fb21600db2e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "65162-541", "generic_name": "Cyclobenzaprine Hydrochloride", "labeler_name": "Amneal Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclobenzaprine Hydrochloride", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA078218", "marketing_category": "ANDA", "marketing_start_date": "20100218", "listing_expiration_date": "20261231"}