Package 42858-102-50

{"route": ["ORAL"], "spl_id": "740ff0d9-308f-487c-90a8-24c8a1b78b65", "openfda": {"unii": ["C1ENJ2TE6C", "362O9ITL9D"], "rxcui": ["1049214", "1049221", "1049225"], "spl_set_id": ["5999f3c3-3225-4d24-82cd-0b8d7a309587"], "manufacturer_name": ["Rhodes Pharmaceuticals L.P."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (42858-102-01)", "package_ndc": "42858-102-01", "marketing_start_date": "20140828"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (42858-102-10)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "42858-102-10", "marketing_start_date": "20140828"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (42858-102-50)", "package_ndc": "42858-102-50", "marketing_start_date": "20140828"}], "brand_name": "Oxycodone and Acetaminophen", "product_id": "42858-102_740ff0d9-308f-487c-90a8-24c8a1b78b65", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "42858-102", "dea_schedule": "CII", "generic_name": "Oxycodone and Acetaminophen", "labeler_name": "Rhodes Pharmaceuticals L.P.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone and Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "OXYCODONE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA201278", "marketing_category": "ANDA", "marketing_start_date": "20140828", "listing_expiration_date": "20271231"}