Package 58657-505-08

Brand: guaifenesin and dextromethorphan hydrobromide

Generic: guaifenesin and dextromethorphan hydrobromide
NDC Package

Package Facts

Identity

Package NDC 58657-505-08
Digits Only 5865750508
Product NDC 58657-505
Description

237 mL in 1 BOTTLE, PLASTIC (58657-505-08)

Marketing

Marketing Status
Marketed Since 2016-06-14
Brand guaifenesin and dextromethorphan hydrobromide
Generic guaifenesin and dextromethorphan hydrobromide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "41b5005a-2f6d-775b-e063-6294a90aa66e", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["996520"], "spl_set_id": ["389230e5-775e-5b0d-e054-00144ff88e88"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Method Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "237 mL in 1 BOTTLE, PLASTIC (58657-505-08)", "package_ndc": "58657-505-08", "marketing_start_date": "20160614"}], "brand_name": "Guaifenesin and Dextromethorphan Hydrobromide", "product_id": "58657-505_41b5005a-2f6d-775b-e063-6294a90aa66e", "dosage_form": "SYRUP", "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": "58657-505", "generic_name": "Guaifenesin and Dextromethorphan Hydrobromide", "labeler_name": "Method Pharmaceuticals", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Guaifenesin and Dextromethorphan Hydrobromide", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "10 mg/5mL"}, {"name": "GUAIFENESIN", "strength": "100 mg/5mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20160614", "listing_expiration_date": "20261231"}