Package 72162-1998-5

{"route": ["ORAL"], "spl_id": "83bd7f0c-95c6-4d46-9ffb-6dba786fb491", "openfda": {"unii": ["362O9ITL9D", "NO70W886KK"], "rxcui": ["856980"], "spl_set_id": ["1170f2f0-f087-4b68-afb5-7c049cb9a619"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-1998-1)", "package_ndc": "72162-1998-1", "marketing_start_date": "20240206"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (72162-1998-5)", "package_ndc": "72162-1998-5", "marketing_start_date": "20240206"}], "brand_name": "hydrocodone bitartrate and acetaminophen", "product_id": "72162-1998_83bd7f0c-95c6-4d46-9ffb-6dba786fb491", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "72162-1998", "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": "10 mg/1"}], "application_number": "ANDA207509", "marketing_category": "ANDA", "marketing_start_date": "20190617", "listing_expiration_date": "20261231"}