Package 83324-026-06

{"route": ["ORAL"], "spl_id": "a2795bf5-34c6-4de6-b9e5-53a23d18e357", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1020138"], "spl_set_id": ["a2795bf5-34c6-4de6-b9e5-53a23d18e357"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Chain Drug Marketing Association Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "177 mL in 1 BOTTLE (83324-026-06)", "package_ndc": "83324-026-06", "marketing_start_date": "20240426"}], "brand_name": "QCH Maximum Strength Mucus Relief DM 628", "product_id": "83324-026_a2795bf5-34c6-4de6-b9e5-53a23d18e357", "dosage_form": "LIQUID", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]", "Sigma-1 Agonist [EPC]", "Sigma-1 Receptor Agonists [MoA]", "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]", "Uncompetitive NMDA Receptor Antagonists [MoA]"], "product_ndc": "83324-026", "generic_name": "Dextromethorphan HBr, Guaifenesin", "labeler_name": "Chain Drug Marketing Association Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "QCH Maximum Strength Mucus Relief DM 628", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "20 mg/20mL"}, {"name": "GUAIFENESIN", "strength": "400 mg/20mL"}], "application_number": "part341", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240426", "listing_expiration_date": "20261231"}