Package 41250-261-34

Brand: adult dm max cough and chest congestion

Generic: dextromethorphan hbr, guaifenesin
NDC Package

Package Facts

Identity

Package NDC 41250-261-34
Digits Only 4125026134
Product NDC 41250-261
Description

1 BOTTLE in 1 CARTON (41250-261-34) / 237 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2018-07-09
Brand adult dm max cough and chest congestion
Generic dextromethorphan hbr, guaifenesin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "5db675c2-0148-4ed7-8959-aea8b425e82d", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1020138"], "spl_set_id": ["3a6855c1-da6d-4fa9-81fe-d2e61355989f"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Meijer Distribution Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (41250-261-34)  / 237 mL in 1 BOTTLE", "package_ndc": "41250-261-34", "marketing_start_date": "20180709"}], "brand_name": "adult dm max cough and chest congestion", "product_id": "41250-261_5db675c2-0148-4ed7-8959-aea8b425e82d", "dosage_form": "SOLUTION", "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": "41250-261", "generic_name": "Dextromethorphan HBr, Guaifenesin", "labeler_name": "Meijer Distribution Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "adult dm max cough and chest congestion", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "20 mg/20mL"}, {"name": "GUAIFENESIN", "strength": "400 mg/20mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180709", "listing_expiration_date": "20261231"}