Package 69168-432-26

{"route": ["ORAL"], "spl_id": "751cf188-7b5f-4f9d-ba3e-8ce7997ecd31", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1147685"], "spl_set_id": ["731f8608-ad5b-491e-a4d4-2bb0c423fed5"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Allegiant Health"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET in 1 BOTTLE (69168-432-06)", "package_ndc": "69168-432-06", "marketing_start_date": "20231106"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (69168-432-07)  / 10 TABLET in 1 BOTTLE", "package_ndc": "69168-432-07", "marketing_start_date": "20220518"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (69168-432-26)  / 20 TABLET in 1 BOTTLE", "package_ndc": "69168-432-26", "marketing_start_date": "20220518"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (69168-432-30)", "package_ndc": "69168-432-30", "marketing_start_date": "20231106"}, {"sample": false, "description": "50 TABLET in 1 BOTTLE (69168-432-50)", "package_ndc": "69168-432-50", "marketing_start_date": "20220608"}, {"sample": false, "description": "200 TABLET in 1 BOTTLE (69168-432-98)", "package_ndc": "69168-432-98", "marketing_start_date": "20220518"}], "brand_name": "Mucus Relief DM Immediate Release", "product_id": "69168-432_751cf188-7b5f-4f9d-ba3e-8ce7997ecd31", "dosage_form": "TABLET", "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": "69168-432", "generic_name": "Mucus Relief DM", "labeler_name": "Allegiant Health", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief DM", "brand_name_suffix": "Immediate Release", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "20 mg/1"}, {"name": "GUAIFENESIN", "strength": "400 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20220518", "listing_expiration_date": "20261231"}