Package 63654-342-20
Brand: mucus relief xpect
Generic: guaifensin, dextromethorphanPackage Facts
Identity
Package NDC
63654-342-20
Digits Only
6365434220
Product NDC
63654-342
Description
2 BLISTER PACK in 1 CARTON (63654-342-20) / 10 TABLET in 1 BLISTER PACK
Marketing
Marketing Status
Brand
mucus relief xpect
Generic
guaifensin, dextromethorphan
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "24b1f277-d157-6ef4-e063-6294a90a15c4", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1147685"], "spl_set_id": ["c2b49d10-b60f-3072-e053-2a95a90af004"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Selder, S.A. de C.V."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (63654-342-20) / 10 TABLET in 1 BLISTER PACK", "package_ndc": "63654-342-20", "marketing_start_date": "20210519"}, {"sample": false, "description": "3 BLISTER PACK in 1 CARTON (63654-342-30) / 10 TABLET in 1 BLISTER PACK", "package_ndc": "63654-342-30", "marketing_start_date": "20210519"}], "brand_name": "Mucus Relief Xpect", "product_id": "63654-342_24b1f277-d157-6ef4-e063-6294a90a15c4", "dosage_form": "TABLET", "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": "63654-342", "generic_name": "Guaifensin, Dextromethorphan", "labeler_name": "Selder, S.A. de C.V.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief Xpect", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "20 mg/1"}, {"name": "GUAIFENESIN", "strength": "400 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210517", "listing_expiration_date": "20261231"}