Package 71930-045-12

{"route": ["ORAL"], "spl_id": "3dba33c1-5d2b-49d4-becb-345947236687", "openfda": {"upc": ["0371930045127", "0371930046124", "0371930047121"], "unii": ["C1ENJ2TE6C", "362O9ITL9D"], "rxcui": ["1049214", "1049221", "1049225"], "spl_set_id": ["1da85ac1-46a2-4081-b533-4890ec9e0482"], "manufacturer_name": ["Eywa Pharma Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (71930-045-12)", "package_ndc": "71930-045-12", "marketing_start_date": "20190601"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (71930-045-52)", "package_ndc": "71930-045-52", "marketing_start_date": "20190601"}], "brand_name": "OXYCODONE AND ACETAMINOPHEN", "product_id": "71930-045_3dba33c1-5d2b-49d4-becb-345947236687", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "71930-045", "dea_schedule": "CII", "generic_name": "oxycodone and acetaminophen", "labeler_name": "Eywa Pharma Inc", "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": "ANDA207510", "marketing_category": "ANDA", "marketing_start_date": "20190601", "listing_expiration_date": "20261231"}