Package 73581-401-70

{"route": ["ORAL"], "spl_id": "4497c67f-376c-7ef0-e063-6294a90ad64a", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0373581000159", "0373581000678"], "unii": ["495W7451VQ"], "rxcui": ["636522"], "spl_set_id": ["d9d1ce2d-d96a-4950-e053-2995a90ad988"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["YYBA CORP"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 TABLET in 1 BOTTLE (73581-401-02)", "package_ndc": "73581-401-02", "marketing_start_date": "20220302"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (73581-401-20)", "package_ndc": "73581-401-20", "marketing_start_date": "20251127"}, {"sample": false, "description": "70 TABLET in 1 BOTTLE (73581-401-70)", "package_ndc": "73581-401-70", "marketing_start_date": "20250102"}], "brand_name": "MUCUS RELIEF GUAIFENESIN EXTENDED-RELEASE 600 mg", "product_id": "73581-401_4497c67f-376c-7ef0-e063-6294a90ad64a", "dosage_form": "TABLET", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "73581-401", "generic_name": "GUAIFENESIN", "labeler_name": "YYBA CORP", "product_type": "HUMAN OTC DRUG", "brand_name_base": "MUCUS RELIEF", "brand_name_suffix": "GUAIFENESIN EXTENDED-RELEASE 600 mg", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "600 mg/1"}], "application_number": "ANDA213420", "marketing_category": "ANDA", "marketing_start_date": "20220302", "listing_expiration_date": "20261231"}