Package 68071-4853-2

{"route": ["ORAL"], "spl_id": "1ae18e8c-cbcd-c096-e063-6394a90a6c48", "openfda": {"upc": ["0368071485325"], "unii": ["362O9ITL9D", "NO70W886KK"], "rxcui": ["857002"], "spl_set_id": ["86be8920-2f35-fbc3-e053-2991aa0a0015"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE (68071-4853-2)", "package_ndc": "68071-4853-2", "marketing_start_date": "20190417"}], "brand_name": "Hydrocodone Bitartrate and Acetaminophen", "product_id": "68071-4853_1ae18e8c-cbcd-c096-e063-6394a90a6c48", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "68071-4853", "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": "5 mg/1"}], "application_number": "ANDA201013", "marketing_category": "ANDA", "marketing_start_date": "20120411", "listing_expiration_date": "20261231"}