Package 65862-922-01

{"route": ["ORAL"], "spl_id": "e0a5c380-895e-4f05-9eaf-b27b17ad41e1", "openfda": {"unii": ["362O9ITL9D", "9N7R477WCK"], "rxcui": ["836395"], "spl_set_id": ["6c2894df-eeeb-4b22-ab32-8ce1601bfdfa"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (65862-922-01)", "package_ndc": "65862-922-01", "marketing_start_date": "20170322"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (65862-922-05)", "package_ndc": "65862-922-05", "marketing_start_date": "20170322"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (65862-922-30)", "package_ndc": "65862-922-30", "marketing_start_date": "20170322"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (65862-922-78)  / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-922-10)", "package_ndc": "65862-922-78", "marketing_start_date": "20170322"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (65862-922-99)", "package_ndc": "65862-922-99", "marketing_start_date": "20170322"}], "brand_name": "Tramadol Hydrochloride and Acetaminophen", "product_id": "65862-922_e0a5c380-895e-4f05-9eaf-b27b17ad41e1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "65862-922", "dea_schedule": "CIV", "generic_name": "Tramadol Hydrochloride and Acetaminophen", "labeler_name": "Aurobindo Pharma Limited", "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": "ANDA207152", "marketing_category": "ANDA", "marketing_start_date": "20170322", "listing_expiration_date": "20261231"}