Package 69420-1001-3

{"route": ["ORAL"], "spl_id": "e28f3c02-e3b3-44e6-895e-40f161d383c0", "openfda": {"upc": ["0369420100111", "0369420100135"], "unii": ["0VE05JYS2P"], "rxcui": ["828299"], "spl_set_id": ["a4ae481f-9e47-470a-b4d1-5a33c0df8761"], "manufacturer_name": ["SA3, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (69420-1001-1)", "package_ndc": "69420-1001-1", "marketing_start_date": "20150325"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (69420-1001-2)", "package_ndc": "69420-1001-2", "marketing_start_date": "20150325"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (69420-1001-3)", "package_ndc": "69420-1001-3", "marketing_start_date": "20150325"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "69420-1001_e28f3c02-e3b3-44e6-895e-40f161d383c0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "69420-1001", "generic_name": "Cyclobenzaprine Hydrochloride", "labeler_name": "SA3, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclobenzaprine Hydrochloride", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "7.5 mg/1"}], "application_number": "ANDA078722", "marketing_category": "ANDA", "marketing_start_date": "20150325", "listing_expiration_date": "20261231"}