Package 31722-942-05

{"route": ["ORAL"], "spl_id": "a80ded9e-2f30-4db6-89ac-07af3d13c6b7", "openfda": {"upc": ["0331722940016", "0331722942010"], "unii": ["NO70W886KK", "362O9ITL9D"], "rxcui": ["857005", "857391"], "spl_set_id": ["4d5bfd3a-3793-4d24-aedd-c04fa34ea736"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (31722-942-01)", "package_ndc": "31722-942-01", "marketing_start_date": "20250822"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (31722-942-05)", "package_ndc": "31722-942-05", "marketing_start_date": "20250822"}], "brand_name": "Hydrocodone Bitartrate and Acetaminophen", "product_id": "31722-942_a80ded9e-2f30-4db6-89ac-07af3d13c6b7", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "31722-942", "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": "7.5 mg/1"}], "application_number": "ANDA211487", "marketing_category": "ANDA", "marketing_start_date": "20250822", "listing_expiration_date": "20261231"}