Package 82442-741-58

{"route": ["ORAL"], "spl_id": "3c75711c-056e-4861-a6a0-100797212454", "openfda": {"nui": ["N0000175706", "M0014836"], "unii": ["6M3C89ZY6R"], "rxcui": ["359818"], "spl_set_id": ["65a612e8-18d3-49fd-844f-4ccd0210acd3"], "pharm_class_cs": ["Nicotine [CS]"], "pharm_class_epc": ["Cholinergic Nicotinic Agonist [EPC]"], "manufacturer_name": ["Target Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 CONTAINER in 1 CARTON (82442-741-27)  / 40 LOZENGE in 1 CONTAINER", "package_ndc": "82442-741-27", "marketing_start_date": "20240212"}, {"sample": false, "description": "40 LOZENGE in 1 CONTAINER (82442-741-58)", "package_ndc": "82442-741-58", "marketing_start_date": "20240212"}], "brand_name": "up and up nicotine", "product_id": "82442-741_3c75711c-056e-4861-a6a0-100797212454", "dosage_form": "LOZENGE", "pharm_class": ["Cholinergic Nicotinic Agonist [EPC]", "Nicotine [CS]"], "product_ndc": "82442-741", "generic_name": "nicotine polacrilex", "labeler_name": "Target Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "up and up nicotine", "active_ingredients": [{"name": "NICOTINE", "strength": "4 mg/1"}], "application_number": "ANDA077007", "marketing_category": "ANDA", "marketing_start_date": "20240212", "listing_expiration_date": "20261231"}