Package 65162-207-10

{"route": ["ORAL"], "spl_id": "34daf86b-3616-4e9e-a43e-56666cf95fa4", "openfda": {"upc": ["0365162207101"], "unii": ["362O9ITL9D", "C1ENJ2TE6C"], "rxcui": ["1049225"], "spl_set_id": ["c5cc2e88-aa00-46bd-91dc-901c3a7c899c"], "manufacturer_name": ["Amneal Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (65162-207-03)", "package_ndc": "65162-207-03", "marketing_start_date": "20131101"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (65162-207-10)", "package_ndc": "65162-207-10", "marketing_start_date": "20131101"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (65162-207-50)", "package_ndc": "65162-207-50", "marketing_start_date": "20131101"}], "brand_name": "Oxycodone and Acetaminophen", "product_id": "65162-207_34daf86b-3616-4e9e-a43e-56666cf95fa4", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "65162-207", "dea_schedule": "CII", "generic_name": "Oxycodone and Acetaminophen", "labeler_name": "Amneal Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone and Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "OXYCODONE HYDROCHLORIDE", "strength": "7.5 mg/1"}], "application_number": "ANDA040778", "marketing_category": "ANDA", "marketing_start_date": "20131101", "listing_expiration_date": "20271231"}