Package 69729-783-02

Brand: guaifenesin, dextromethorphan hbr

Generic: guaifenesin, dextromethorphan hbr
NDC Package

Package Facts

Identity

Package NDC 69729-783-02
Digits Only 6972978302
Product NDC 69729-783
Description

2 BLISTER PACK in 1 CARTON (69729-783-02) / 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2019-02-18
Brand guaifenesin, dextromethorphan hbr
Generic guaifenesin, dextromethorphan hbr
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "18aab413-451c-bdd4-e063-6394a90a3eb6", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0856828008434"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1661740"], "spl_set_id": ["9a246099-72b5-2efc-e053-2a95a90aafbc"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["OPMX LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (69729-783-02)  / 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK", "package_ndc": "69729-783-02", "marketing_start_date": "20190218"}], "brand_name": "GUAIFENESIN, DEXTROMETHORPHAN HBR", "product_id": "69729-783_18aab413-451c-bdd4-e063-6394a90a3eb6", "dosage_form": "CAPSULE, LIQUID FILLED", "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": "69729-783", "generic_name": "GUAIFENESIN, DEXTROMETHORPHAN HBR", "labeler_name": "OPMX LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "GUAIFENESIN, DEXTROMETHORPHAN HBR", "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": "20190218", "listing_expiration_date": "20261231"}