Package 68016-293-44

{"route": ["BUCCAL"], "spl_id": "db508300-2736-4906-b159-8746bc1c1d6e", "openfda": {"nui": ["N0000175706", "M0014836"], "upc": ["0840986034862"], "unii": ["6M3C89ZY6R"], "rxcui": ["311975", "314119"], "spl_set_id": ["9c115cd5-1952-4f1e-8e88-27f2c528e91f"], "pharm_class_cs": ["Nicotine [CS]"], "pharm_class_epc": ["Cholinergic Nicotinic Agonist [EPC]"], "manufacturer_name": ["Chain Drug Consortium, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (68016-293-44)  / 1 GUM, CHEWING in 1 BLISTER PACK", "package_ndc": "68016-293-44", "marketing_end_date": "20261231", "marketing_start_date": "20171001"}], "brand_name": "Nicotine Polacrilex", "product_id": "68016-293_db508300-2736-4906-b159-8746bc1c1d6e", "dosage_form": "GUM, CHEWING", "pharm_class": ["Cholinergic Nicotinic Agonist [EPC]", "Nicotine [CS]"], "product_ndc": "68016-293", "generic_name": "Nicotine Polacrilex", "labeler_name": "Chain Drug Consortium, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Nicotine Polacrilex", "active_ingredients": [{"name": "NICOTINE", "strength": "4 mg/1"}], "application_number": "ANDA204833", "marketing_category": "ANDA", "marketing_end_date": "20261231", "marketing_start_date": "20171001"}