Package 76095-012-20
Brand: mucus relief xpect
Generic: guaifensin, dextromethorphanPackage Facts
Identity
Package NDC
76095-012-20
Digits Only
7609501220
Product NDC
76095-012
Description
2 BLISTER PACK in 1 CARTON (76095-012-20) / 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": "24b26929-2f23-e5e7-e063-6394a90af59a", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1147685"], "spl_set_id": ["c2c8bd26-bbf1-c2e6-e053-2995a90a86a7"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Midway Importing Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (76095-012-20) / 10 TABLET in 1 BLISTER PACK", "package_ndc": "76095-012-20", "marketing_start_date": "20210519"}, {"sample": false, "description": "3 BLISTER PACK in 1 CARTON (76095-012-30) / 10 TABLET in 1 BLISTER PACK", "package_ndc": "76095-012-30", "marketing_start_date": "20210519"}], "brand_name": "Mucus Relief Xpect", "product_id": "76095-012_24b26929-2f23-e5e7-e063-6394a90af59a", "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": "76095-012", "generic_name": "Guaifensin, Dextromethorphan", "labeler_name": "Midway Importing Inc.", "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"}