Package 0113-0927-26
Brand: good sense tussin dm max
Generic: dextromethorphan hbr, guaifenesinPackage Facts
Identity
Package NDC
0113-0927-26
Digits Only
0113092726
Product NDC
0113-0927
Description
1 BOTTLE in 1 CARTON (0113-0927-26) / 118 mL in 1 BOTTLE
Marketing
Marketing Status
Brand
good sense tussin dm max
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": "5129c8fe-a209-476c-9bc0-2b362f7b5386", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1020138"], "spl_set_id": ["d2541ef0-a73c-43aa-91ff-fdbce2748c4f"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["L. Perrigo Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0113-0927-26) / 118 mL in 1 BOTTLE", "package_ndc": "0113-0927-26", "marketing_start_date": "20180806"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0113-0927-34) / 237 mL in 1 BOTTLE", "package_ndc": "0113-0927-34", "marketing_start_date": "20180801"}], "brand_name": "Good Sense Tussin DM Max", "product_id": "0113-0927_5129c8fe-a209-476c-9bc0-2b362f7b5386", "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": "0113-0927", "generic_name": "Dextromethorphan HBr, Guaifenesin", "labeler_name": "L. Perrigo Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Good Sense 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": "20180801", "listing_expiration_date": "20261231"}