Package 72162-1989-1

{"route": ["ORAL"], "spl_id": "b7066906-2a64-48fd-849c-4ae545026e26", "openfda": {"unii": ["362O9ITL9D", "NO70W886KK"], "rxcui": ["857002"], "spl_set_id": ["db14e63a-8e3e-4524-b45a-cb09f705f73a"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-1989-1)", "package_ndc": "72162-1989-1", "marketing_start_date": "20180713"}], "brand_name": "Hydrocodone Bitartrate and Acetaminophen", "product_id": "72162-1989_b7066906-2a64-48fd-849c-4ae545026e26", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "72162-1989", "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": "5 mg/1"}], "application_number": "ANDA210211", "marketing_category": "ANDA", "marketing_start_date": "20180713", "listing_expiration_date": "20261231"}