Package 69729-040-04
Brand: dextromethorphan hydrobromide and guaifenesin
Generic: dextromethorphan hydrobromide and guaifenesinPackage Facts
Identity
Package NDC
69729-040-04
Digits Only
6972904004
Product NDC
69729-040
Description
118 mL in 1 BOTTLE (69729-040-04)
Marketing
Marketing Status
Brand
dextromethorphan hydrobromide and guaifenesin
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": "352f8de3-8fe0-4098-e063-6294a90ace4d", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0810053180099", "0810053180235", "0856828008502"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1117394"], "spl_set_id": ["826c2f47-00a6-4060-a7ad-1ef26ccfddd1"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["OPMX LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "118 mL in 1 BOTTLE (69729-040-04)", "package_ndc": "69729-040-04", "marketing_start_date": "20210201"}], "brand_name": "DEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN", "product_id": "69729-040_352f8de3-8fe0-4098-e063-6294a90ace4d", "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": "69729-040", "generic_name": "DEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN", "labeler_name": "OPMX LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "DEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "20 mg/5mL"}, {"name": "GUAIFENESIN", "strength": "300 mg/5mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210201", "listing_expiration_date": "20261231"}