Package 16571-783-01

{"route": ["ORAL"], "spl_id": "0280b504-4a42-44f3-8a1a-34a20eac054a", "openfda": {"upc": ["0316571782017", "0316571783014"], "unii": ["0VE05JYS2P"], "rxcui": ["828320", "828348"], "spl_set_id": ["0280b504-4a42-44f3-8a1a-34a20eac054a"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (16571-783-01)", "package_ndc": "16571-783-01", "marketing_start_date": "20080926"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (16571-783-10)", "package_ndc": "16571-783-10", "marketing_start_date": "20080926"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (16571-783-50)", "package_ndc": "16571-783-50", "marketing_start_date": "20080926"}], "brand_name": "Cyclobenzaprine Hydrochloride", "product_id": "16571-783_0280b504-4a42-44f3-8a1a-34a20eac054a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "16571-783", "generic_name": "Cyclobenzaprine Hydrochloride", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cyclobenzaprine Hydrochloride", "active_ingredients": [{"name": "CYCLOBENZAPRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA078643", "marketing_category": "ANDA", "marketing_start_date": "20080926", "listing_expiration_date": "20261231"}