Package 72865-111-05

{"route": ["ORAL"], "spl_id": "fe42cdff-62f7-4209-b953-1f4d13ba4195", "openfda": {"upc": ["0372865111017", "0372865112014", "0372865109014", "0372865110010"], "unii": ["NO70W886KK", "362O9ITL9D"], "rxcui": ["856999", "857002", "857005", "857391"], "spl_set_id": ["73dea6de-20cb-4cef-b987-3ab2c64e5edb"], "manufacturer_name": ["XLCare Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72865-111-01)", "package_ndc": "72865-111-01", "marketing_start_date": "20200227"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (72865-111-05)", "package_ndc": "72865-111-05", "marketing_start_date": "20200227"}], "brand_name": "Hydrocodone Bitartrate and Acetaminophen", "product_id": "72865-111_fe42cdff-62f7-4209-b953-1f4d13ba4195", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "72865-111", "dea_schedule": "CII", "generic_name": "Hydrocodone Bitartrate and Acetaminophen", "labeler_name": "XLCare Pharmaceuticals, Inc.", "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": "ANDA211487", "marketing_category": "ANDA", "marketing_start_date": "20200227", "listing_expiration_date": "20261231"}