Package 83324-023-04
Brand: qch adult tussin dm 542
Generic: dextromethorphan hbr, guaifenesinPackage Facts
Identity
Package NDC
83324-023-04
Digits Only
8332402304
Product NDC
83324-023
Description
1 BOTTLE in 1 CARTON (83324-023-04) / 118 mL in 1 BOTTLE
Marketing
Marketing Status
Brand
qch adult tussin dm 542
Generic
dextromethorphan hbr, guaifenesin
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "41a95b6d-6e0a-4729-ac06-3963a78a0e51", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1790650"], "spl_set_id": ["17caffa4-a264-7f3e-e063-6394a90ac419"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Chain Drug Marketing Association Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (83324-023-04) / 118 mL in 1 BOTTLE", "package_ndc": "83324-023-04", "marketing_start_date": "20240508"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (83324-023-08) / 237 mL in 1 BOTTLE", "package_ndc": "83324-023-08", "marketing_start_date": "20240508"}], "brand_name": "QCH Adult Tussin DM 542", "product_id": "83324-023_41a95b6d-6e0a-4729-ac06-3963a78a0e51", "dosage_form": "LIQUID", "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": "83324-023", "generic_name": "Dextromethorphan HBr, Guaifenesin", "labeler_name": "Chain Drug Marketing Association Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "QCH Adult Tussin DM 542", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "20 mg/20mL"}, {"name": "GUAIFENESIN", "strength": "200 mg/20mL"}], "application_number": "part341", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240508", "listing_expiration_date": "20261231"}