Package 0406-0512-91

{"route": ["ORAL"], "spl_id": "38cc2423-8e75-4007-b224-75aa920582d7", "openfda": {"upc": ["0304060522053", "0304060523050", "0304060512054"], "unii": ["C1ENJ2TE6C", "362O9ITL9D"], "rxcui": ["1049214", "1049221", "1049225"], "spl_set_id": ["f2137f1a-b49a-40bd-97ac-cd6b36e295f4"], "manufacturer_name": ["SpecGx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0406-0512-01)", "package_ndc": "0406-0512-01", "marketing_start_date": "19831207"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (0406-0512-05)", "package_ndc": "0406-0512-05", "marketing_start_date": "19831207"}, {"sample": false, "description": "1 TABLET in 1 BLISTER PACK (0406-0512-23)", "package_ndc": "0406-0512-23", "marketing_start_date": "19831207"}, {"sample": false, "description": "100 TABLET in 1 BLISTER PACK (0406-0512-62)", "package_ndc": "0406-0512-62", "marketing_start_date": "19831207"}, {"sample": false, "description": "5000 TABLET in 1 PAIL (0406-0512-91)", "package_ndc": "0406-0512-91", "marketing_start_date": "19831207"}], "brand_name": "OXYCODONE AND ACETAMINOPHEN", "product_id": "0406-0512_38cc2423-8e75-4007-b224-75aa920582d7", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "0406-0512", "dea_schedule": "CII", "generic_name": "oxycodone hydrochloride and acetaminophen", "labeler_name": "SpecGx LLC", "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": "ANDA087463", "marketing_category": "ANDA", "marketing_start_date": "19831207", "listing_expiration_date": "20271231"}