Package 53746-204-01

{"route": ["ORAL"], "spl_id": "be8f26ed-3ee9-4a9f-b300-8c7654a84ceb", "openfda": {"upc": ["0353746204011"], "unii": ["362O9ITL9D", "C1ENJ2TE6C"], "rxcui": ["1049214"], "spl_set_id": ["d61e0ff4-e04b-4dc6-b818-6a8f46e99b5e"], "manufacturer_name": ["Amneal Pharmaceuticals of New York LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (53746-204-01)", "package_ndc": "53746-204-01", "marketing_start_date": "20071127"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (53746-204-05)", "package_ndc": "53746-204-05", "marketing_start_date": "20071127"}], "brand_name": "Oxycodone and Acetaminophen", "product_id": "53746-204_be8f26ed-3ee9-4a9f-b300-8c7654a84ceb", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "53746-204", "dea_schedule": "CII", "generic_name": "Oxycodone and Acetaminophen", "labeler_name": "Amneal Pharmaceuticals of New York LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone and Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "OXYCODONE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA040778", "marketing_category": "ANDA", "marketing_start_date": "20071127", "listing_expiration_date": "20271231"}