Package 72090-044-02

{"route": ["ORAL"], "spl_id": "5b76710f-94ab-442e-8acd-e4f8324272ad", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0372090002975"], "unii": ["495W7451VQ"], "rxcui": ["359601"], "spl_set_id": ["729ab412-f30b-4ad1-9d8f-1a5e1c48b118"], "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": "300 TABLET in 1 BOTTLE (72090-044-02)", "package_ndc": "72090-044-02", "marketing_start_date": "20250416"}], "brand_name": "MUCUS RELIEF", "product_id": "72090-044_5b76710f-94ab-442e-8acd-e4f8324272ad", "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": "20250416", "listing_expiration_date": "20261231"}