Package 68071-2645-2

{"route": ["ORAL"], "spl_id": "2a09ec53-48b8-1bf1-e063-6294a90a6e69", "openfda": {"upc": ["0368071264531"], "unii": ["362O9ITL9D", "NO70W886KK"], "rxcui": ["857005"], "spl_set_id": ["d88e04c1-cd54-6a12-e053-2995a90a22b4"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE (68071-2645-2)", "package_ndc": "68071-2645-2", "marketing_start_date": "20240628"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-2645-3)", "package_ndc": "68071-2645-3", "marketing_start_date": "20220221"}], "brand_name": "Hydrocodone Bitartrate and Acetaminophen", "product_id": "68071-2645_2a09ec53-48b8-1bf1-e063-6294a90a6e69", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "68071-2645", "dea_schedule": "CII", "generic_name": "Hydrocodone Bitartrate and Acetaminophen", "labeler_name": "NuCare 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": "ANDA210211", "marketing_category": "ANDA", "marketing_start_date": "20180713", "listing_expiration_date": "20261231"}