Package 55681-311-03

{"route": ["ORAL"], "spl_id": "3906e938-65b3-d3e3-e063-6294a90a3020", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0816516015496"], "unii": ["495W7451VQ"], "rxcui": ["359601"], "spl_set_id": ["e31bd69f-97ab-9d99-e053-2995a90a580e"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["TWIN MED LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "300 TABLET in 1 BOTTLE (55681-311-03)", "package_ndc": "55681-311-03", "marketing_start_date": "20220701"}], "brand_name": "Mucus Relief", "product_id": "55681-311_3906e938-65b3-d3e3-e063-6294a90a3020", "dosage_form": "TABLET", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "55681-311", "generic_name": "Guaifenesin 400 mg", "labeler_name": "TWIN MED LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "400 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20220701", "listing_expiration_date": "20261231"}