Package 85722-0001-8

Brand: dextromethorphan hydrobromide and guaifenesin

Generic: dextromethorphan hydrobromide and guaifenesin
NDC Package

Package Facts

Identity

Package NDC 85722-0001-8
Digits Only 8572200018
Product NDC 85722-0001
Description

236 mL in 1 BOTTLE (85722-0001-8)

Marketing

Marketing Status
Marketed Since 2021-02-01
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": "a2cca1a0-64ab-4650-beb5-1265425eac7b", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["996520"], "spl_set_id": ["8877bb8d-479f-4968-8033-5c269d449a46"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["KJD Pharma Private Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "118 mL in 1 BOTTLE (85722-0001-4)", "package_ndc": "85722-0001-4", "marketing_start_date": "20210201"}, {"sample": false, "description": "473 mL in 1 BOTTLE (85722-0001-6)", "package_ndc": "85722-0001-6", "marketing_start_date": "20210201"}, {"sample": false, "description": "236 mL in 1 BOTTLE (85722-0001-8)", "package_ndc": "85722-0001-8", "marketing_start_date": "20210201"}], "brand_name": "DEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN", "product_id": "85722-0001_a2cca1a0-64ab-4650-beb5-1265425eac7b", "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": "85722-0001", "generic_name": "DEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN", "labeler_name": "KJD Pharma Private Limited", "product_type": "HUMAN OTC DRUG", "brand_name_base": "DEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN", "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": "20210201", "listing_expiration_date": "20261231"}