Package 55505-231-24
Brand: safetussin non drowsy cough plus chest congestion
Generic: dextromethorphan hydrobromide, and guaifenesinPackage 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
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"}