Package 0904-7093-61

{"route": ["ORAL"], "spl_id": "92f33065-bd48-442a-942c-088d790b955d", "openfda": {"unii": ["C1ENJ2TE6C", "362O9ITL9D"], "rxcui": ["1049214", "1049221", "1049225"], "spl_set_id": ["1d52272f-a607-4002-a61c-341964522b82"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-7093-61)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0904-7093-61", "marketing_start_date": "20190601"}], "brand_name": "OXYCODONE AND ACETAMINOPHEN", "product_id": "0904-7093_92f33065-bd48-442a-942c-088d790b955d", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "0904-7093", "dea_schedule": "CII", "generic_name": "oxycodone and acetaminophen", "labeler_name": "Major Pharmaceuticals", "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"}