Package 55505-231-24

Brand: safetussin non drowsy cough plus chest congestion

Generic: dextromethorphan hydrobromide, and guaifenesin
NDC Package

Package Facts

Identity

Package NDC 55505-231-24
Digits Only 5550523124
Product NDC 55505-231
Description

24 TABLET in 1 CARTON (55505-231-24)

Marketing

Marketing Status
Marketed Since 2024-05-17
Brand safetussin non drowsy cough plus chest congestion
Generic dextromethorphan hydrobromide, and guaifenesin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4c618596-e3fe-4557-8ccb-0867ebb871c9", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0053076000092"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["2173726"], "spl_set_id": ["eeca6370-29ea-4540-8139-e8461d58a286"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["KRAMER LABORATORIES"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 TABLET in 1 CARTON (55505-231-24)", "package_ndc": "55505-231-24", "marketing_start_date": "20240517"}], "brand_name": "SAFETUSSIN Non Drowsy Cough plus chest congestion", "product_id": "55505-231_4c618596-e3fe-4557-8ccb-0867ebb871c9", "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": "55505-231", "generic_name": "Dextromethorphan Hydrobromide, and Guaifenesin", "labeler_name": "KRAMER LABORATORIES", "product_type": "HUMAN OTC DRUG", "brand_name_base": "SAFETUSSIN Non Drowsy", "brand_name_suffix": "Cough plus chest congestion", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "10 mg/1"}, {"name": "GUAIFENESIN", "strength": "200 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240517", "listing_expiration_date": "20261231"}