Package 72162-1990-5

{"route": ["ORAL"], "spl_id": "9a07d740-32b5-4ad5-872b-32978b31cb10", "openfda": {"unii": ["362O9ITL9D", "NO70W886KK"], "rxcui": ["857005"], "spl_set_id": ["e5b559c3-4beb-4ba3-a10b-7a1ad1878a1e"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (72162-1990-5)", "package_ndc": "72162-1990-5", "marketing_start_date": "20180713"}], "brand_name": "Hydrocodone Bitartrate and Acetaminophen", "product_id": "72162-1990_9a07d740-32b5-4ad5-872b-32978b31cb10", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "72162-1990", "dea_schedule": "CII", "generic_name": "Hydrocodone Bitartrate and Acetaminophen", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrocodone Bitartrate and Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "HYDROCODONE BITARTRATE", "strength": "7.5 mg/1"}], "application_number": "ANDA210211", "marketing_category": "ANDA", "marketing_start_date": "20180713", "listing_expiration_date": "20261231"}