Package 63824-072-56

Brand: mucinex dm maximum strength

Generic: guaifenesin and dextromethorphan hydrobromide
NDC Package

Package Facts

Identity

Package NDC 63824-072-56
Digits Only 6382407256
Product NDC 63824-072
Description

4 BLISTER PACK in 1 CARTON (63824-072-56) / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2021-07-01
Brand mucinex dm maximum strength
Generic guaifenesin and dextromethorphan hydrobromide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "324b0a12-8964-731d-e063-6394a90a00a7", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0363824072142"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1099074"], "spl_set_id": ["588eddc1-fa30-41cc-8ed9-c01319ea21c6"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["RB Health (US) LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 POUCH in 1 CARTON (63824-072-02)  / 1 TABLET, EXTENDED RELEASE in 1 POUCH", "package_ndc": "63824-072-02", "marketing_start_date": "20210801"}, {"sample": false, "description": "1 BLISTER PACK in 1 CARTON (63824-072-07)  / 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "63824-072-07", "marketing_start_date": "20120626"}, {"sample": false, "description": "1 BLISTER PACK in 1 CARTON (63824-072-35)  / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "63824-072-35", "marketing_start_date": "20120626"}, {"sample": false, "description": "2 BLISTER PACK in 1 CARTON (63824-072-36)  / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "63824-072-36", "marketing_start_date": "20120626"}, {"sample": false, "description": "3 BLISTER PACK in 1 CARTON (63824-072-46)  / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "63824-072-46", "marketing_start_date": "20120626"}, {"sample": false, "description": "4 BLISTER PACK in 1 CARTON (63824-072-48)  / 12 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "63824-072-48", "marketing_start_date": "20120626"}, {"sample": false, "description": "4 BLISTER PACK in 1 CARTON (63824-072-56)  / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "63824-072-56", "marketing_start_date": "20210701"}], "brand_name": "Mucinex DM Maximum Strength", "product_id": "63824-072_324b0a12-8964-731d-e063-6394a90a00a7", "dosage_form": "TABLET, EXTENDED RELEASE", "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": "63824-072", "generic_name": "Guaifenesin and Dextromethorphan Hydrobromide", "labeler_name": "RB Health (US) LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucinex DM", "brand_name_suffix": "Maximum Strength", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "60 mg/1"}, {"name": "GUAIFENESIN", "strength": "1200 mg/1"}], "application_number": "NDA021620", "marketing_category": "NDA", "marketing_start_date": "20120626", "listing_expiration_date": "20261231"}