Package 41163-704-34
Brand: equaline tussin
Generic: dextromethorphan hbr, guaifenesinPackage Facts
Identity
Package NDC
41163-704-34
Digits Only
4116370434
Product NDC
41163-704
Description
1 BOTTLE in 1 CARTON (41163-704-34) / 237 mL in 1 BOTTLE
Marketing
Marketing Status
Brand
equaline tussin
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": "8e74d32e-f53c-4ffe-89c6-844e83bf13e9", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1020138"], "spl_set_id": ["8bc7fa7c-d565-48c9-9808-1042c3e9d428"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["United Natural Foods, Inc. dba UNFI"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (41163-704-26) / 118 mL in 1 BOTTLE", "package_ndc": "41163-704-26", "marketing_start_date": "20180830"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (41163-704-34) / 237 mL in 1 BOTTLE", "package_ndc": "41163-704-34", "marketing_start_date": "20180830"}], "brand_name": "equaline tussin", "product_id": "41163-704_8e74d32e-f53c-4ffe-89c6-844e83bf13e9", "dosage_form": "SOLUTION", "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": "41163-704", "generic_name": "Dextromethorphan HBr, Guaifenesin", "labeler_name": "United Natural Foods, Inc. dba UNFI", "product_type": "HUMAN OTC DRUG", "brand_name_base": "equaline tussin", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "20 mg/20mL"}, {"name": "GUAIFENESIN", "strength": "400 mg/20mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180830", "listing_expiration_date": "20261231"}