Package 29300-355-01

{"route": ["ORAL"], "spl_id": "e0840ce2-185b-4805-874e-9fde301907c4", "openfda": {"upc": ["0329300355017"], "unii": ["9N7R477WCK"], "rxcui": ["835603"], "spl_set_id": ["007bf37f-0e46-426a-ac8c-be63d4b7414c"], "manufacturer_name": ["Unichem Pharmaceuticals (USA), Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-355-01)", "package_ndc": "29300-355-01", "marketing_start_date": "20191104"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-355-05)", "package_ndc": "29300-355-05", "marketing_start_date": "20191104"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-355-10)", "package_ndc": "29300-355-10", "marketing_start_date": "20191104"}], "brand_name": "Tramadol Hydrochloride", "product_id": "29300-355_e0840ce2-185b-4805-874e-9fde301907c4", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "29300-355", "dea_schedule": "CIV", "generic_name": "Tramadol Hydrochloride", "labeler_name": "Unichem Pharmaceuticals (USA), Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tramadol Hydrochloride", "active_ingredients": [{"name": "TRAMADOL HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA211825", "marketing_category": "ANDA", "marketing_start_date": "20190809", "listing_expiration_date": "20271231"}