Package 49348-728-09

Brand: sunmark chest congestion relief dm dm

Generic: dextromethorphan hydrobromide / guaifenesin
NDC Package

Package Facts

Identity

Package NDC 49348-728-09
Digits Only 4934872809
Product NDC 49348-728
Description

1 BOTTLE in 1 CARTON (49348-728-09) / 50 TABLET in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2019-08-29
Brand sunmark chest congestion relief dm dm
Generic dextromethorphan hydrobromide / guaifenesin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e436f142-3bfa-44a0-830f-78ae334c00dd", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1147685"], "spl_set_id": ["10cad9a7-1223-470c-9027-807891217d40"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Strategic Sourcing Services LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (49348-728-09)  / 50 TABLET in 1 BOTTLE", "package_ndc": "49348-728-09", "marketing_start_date": "20190829"}], "brand_name": "Sunmark Chest Congestion Relief DM DM", "product_id": "49348-728_e436f142-3bfa-44a0-830f-78ae334c00dd", "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": "49348-728", "generic_name": "Dextromethorphan Hydrobromide / Guaifenesin", "labeler_name": "Strategic Sourcing Services LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sunmark Chest Congestion Relief DM", "brand_name_suffix": "DM", "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": "20120801", "listing_expiration_date": "20261231"}