Package 31722-997-01

{"route": ["ORAL"], "spl_id": "d745e0ac-ee48-44c7-8430-8da0a69d2735", "openfda": {"upc": ["0331722997010", "0331722996013"], "unii": ["NO70W886KK", "362O9ITL9D"], "rxcui": ["856999", "857002"], "spl_set_id": ["ed6af366-753c-4f3b-a6a2-c9a183c50035"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (31722-997-01)", "package_ndc": "31722-997-01", "marketing_start_date": "20181108"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (31722-997-05)", "package_ndc": "31722-997-05", "marketing_start_date": "20181108"}], "brand_name": "Hydrocodone Bitartrate and Acetaminophen", "product_id": "31722-997_d745e0ac-ee48-44c7-8430-8da0a69d2735", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "31722-997", "dea_schedule": "CII", "generic_name": "Hydrocodone Bitartrate and Acetaminophen", "labeler_name": "Camber 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": "10 mg/1"}], "application_number": "ANDA211487", "marketing_category": "ANDA", "marketing_start_date": "20181108", "listing_expiration_date": "20261231"}