Package 68071-3044-3

{"route": ["ORAL"], "spl_id": "1d8e1fca-6867-7c08-e063-6394a90a08b6", "openfda": {"upc": ["0368071304428"], "unii": ["362O9ITL9D", "9N7R477WCK"], "rxcui": ["836395"], "spl_set_id": ["4a668406-d2fc-13c9-e054-00144ff88e88"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (68071-3044-2)", "package_ndc": "68071-3044-2", "marketing_start_date": "20170310"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68071-3044-3)", "package_ndc": "68071-3044-3", "marketing_start_date": "20170310"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68071-3044-6)", "package_ndc": "68071-3044-6", "marketing_start_date": "20170310"}], "brand_name": "Tramadol Hydrochloride and Acetaminophen", "product_id": "68071-3044_1d8e1fca-6867-7c08-e063-6394a90a08b6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "68071-3044", "dea_schedule": "CIV", "generic_name": "Tramadol Hydrochloride and Acetaminophen", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tramadol Hydrochloride and Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "TRAMADOL HYDROCHLORIDE", "strength": "37.5 mg/1"}], "application_number": "ANDA090460", "marketing_category": "ANDA", "marketing_start_date": "20121015", "listing_expiration_date": "20261231"}