Package 0363-1144-34
Brand: tussin dm max
Generic: dextromethorphan hydrobromide, guaifenesinPackage Facts
Identity
Package NDC
0363-1144-34
Digits Only
0363114434
Product NDC
0363-1144
Description
1 BOTTLE in 1 CARTON (0363-1144-34) / 237 mL in 1 BOTTLE
Marketing
Marketing Status
Brand
tussin dm max
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": "6dca6e0b-1e4e-4d4a-b085-7ae9a0c7fe8a", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1020138"], "spl_set_id": ["756794b0-8d3b-4732-947c-a407caf400e2"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Walgreen Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-1144-26) / 118 mL in 1 BOTTLE", "package_ndc": "0363-1144-26", "marketing_start_date": "20220524"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-1144-34) / 237 mL in 1 BOTTLE", "package_ndc": "0363-1144-34", "marketing_start_date": "20220524"}], "brand_name": "tussin dm max", "product_id": "0363-1144_6dca6e0b-1e4e-4d4a-b085-7ae9a0c7fe8a", "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": "0363-1144", "generic_name": "Dextromethorphan Hydrobromide, Guaifenesin", "labeler_name": "Walgreen Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "tussin dm max", "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": "20220524", "listing_expiration_date": "20261231"}