Package 72090-013-01

{"route": ["ORAL"], "spl_id": "c4e18579-c7f2-4d4c-aacb-b7fe47ab1d12", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["495W7451VQ"], "rxcui": ["359601"], "spl_set_id": ["1194c338-e115-4105-93d8-9ab833c43193"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Pioneer Life Sciences, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 TABLET in 1 BOTTLE (72090-013-01)", "package_ndc": "72090-013-01", "marketing_start_date": "20240119"}], "brand_name": "MUCUS RELIEF", "product_id": "72090-013_c4e18579-c7f2-4d4c-aacb-b7fe47ab1d12", "dosage_form": "TABLET", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "72090-013", "generic_name": "guaifenesin 400 mg", "labeler_name": "Pioneer Life Sciences, 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": "20240119", "listing_expiration_date": "20261231"}