Package 72090-044-01

{"route": ["ORAL"], "spl_id": "3fcd9adf-7b5f-406c-9ab6-3460eb23fe6f", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["495W7451VQ"], "rxcui": ["359601"], "spl_set_id": ["1695e7ea-2f83-4d3a-980e-c91be6c1f2a5"], "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 (72090-044-01)", "package_ndc": "72090-044-01", "marketing_start_date": "20251223"}], "brand_name": "MUCUS RELIEF", "product_id": "72090-044_3fcd9adf-7b5f-406c-9ab6-3460eb23fe6f", "dosage_form": "TABLET", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "72090-044", "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": "20251223", "listing_expiration_date": "20261231"}