Package 70010-672-05

{"route": ["ORAL"], "spl_id": "422263e3-1184-c7ea-e063-6294a90ae818", "openfda": {"upc": ["0370010673014", "0370010674011", "0370010672017"], "unii": ["NO70W886KK", "362O9ITL9D"], "rxcui": ["856999", "857002", "857005"], "spl_set_id": ["136bbd47-7a54-493f-9158-a84d39221d6c"], "manufacturer_name": ["Granules Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (70010-672-01)", "package_ndc": "70010-672-01", "marketing_start_date": "20210818"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (70010-672-05)", "package_ndc": "70010-672-05", "marketing_start_date": "20210818"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (70010-672-10)", "package_ndc": "70010-672-10", "marketing_start_date": "20250606"}], "brand_name": "Hydrocodone Bitartrate and Acetaminophen", "product_id": "70010-672_422263e3-1184-c7ea-e063-6294a90ae818", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "70010-672", "dea_schedule": "CII", "generic_name": "Hydrocodone Bitartrate and Acetaminophen", "labeler_name": "Granules 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": "5 mg/1"}], "application_number": "ANDA211729", "marketing_category": "ANDA", "marketing_start_date": "20210818", "listing_expiration_date": "20261231"}