Package 73581-402-35

{"route": ["ORAL"], "spl_id": "4496da23-2589-3cc4-e063-6394a90a93d9", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0373581000173", "0373581000661"], "unii": ["495W7451VQ"], "rxcui": ["310621"], "spl_set_id": ["d9d2539b-bd31-66bd-e053-2a95a90aa583"], "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": "100 TABLET in 1 BOTTLE (73581-402-01)", "package_ndc": "73581-402-01", "marketing_start_date": "20220302"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (73581-402-10)", "package_ndc": "73581-402-10", "marketing_start_date": "20251127"}, {"sample": false, "description": "35 TABLET in 1 BOTTLE (73581-402-35)", "package_ndc": "73581-402-35", "marketing_start_date": "20250102"}], "brand_name": "MUCUS RELIEF GUAIFENESIN EXTENDED-RELEASE 1200 mg", "product_id": "73581-402_4496da23-2589-3cc4-e063-6394a90a93d9", "dosage_form": "TABLET", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "73581-402", "generic_name": "GUAIFENESIN", "labeler_name": "YYBA CORP", "product_type": "HUMAN OTC DRUG", "brand_name_base": "MUCUS RELIEF", "brand_name_suffix": "GUAIFENESIN EXTENDED-RELEASE 1200 mg", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "1200 mg/1"}], "application_number": "ANDA213420", "marketing_category": "ANDA", "marketing_start_date": "20220302", "listing_expiration_date": "20261231"}