Package 63629-1181-1

{"route": ["ORAL"], "spl_id": "bd61638a-dd44-4d11-a4b1-c8434230b701", "openfda": {"unii": ["NO70W886KK", "362O9ITL9D"], "rxcui": ["856980", "856987", "856992"], "spl_set_id": ["c648e299-2a8b-4530-a061-c6fd9cd1294c"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (63629-1181-1)", "package_ndc": "63629-1181-1", "marketing_start_date": "20200901"}], "brand_name": "hydrocodone bitartrate and acetaminophen", "product_id": "63629-1181_bd61638a-dd44-4d11-a4b1-c8434230b701", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "63629-1181", "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": "300 mg/1"}, {"name": "HYDROCODONE BITARTRATE", "strength": "7.5 mg/1"}], "application_number": "ANDA207509", "marketing_category": "ANDA", "marketing_start_date": "20200901", "listing_expiration_date": "20261231"}