Package 64850-623-01

{"route": ["ORAL"], "spl_id": "6371920d-34a5-41ac-ba08-3b91fd68075b", "openfda": {"upc": ["0364850621014", "0364850622011", "0364850623018"], "unii": ["C1ENJ2TE6C", "362O9ITL9D"], "rxcui": ["1049214", "1049221", "1049225"], "spl_set_id": ["27fa8190-d334-4bb9-b277-d1f44db433e3"], "manufacturer_name": ["Elite Laboratories, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (64850-623-01)", "package_ndc": "64850-623-01", "marketing_start_date": "20171204"}], "brand_name": "Oxycodone Hydrochloride and Acetaminophen", "product_id": "64850-623_6371920d-34a5-41ac-ba08-3b91fd68075b", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "64850-623", "dea_schedule": "CII", "generic_name": "Oxycodone Hydrochloride and Acetaminophen", "labeler_name": "Elite Laboratories, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone Hydrochloride and Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "OXYCODONE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA209385", "marketing_category": "ANDA", "marketing_start_date": "20171204", "listing_expiration_date": "20261231"}