Package 69842-513-34
Brand: adult tussin dm
Generic: dextromethorphan hydrobromide, guaifenesinPackage Facts
Identity
Package NDC
69842-513-34
Digits Only
6984251334
Product NDC
69842-513
Description
1 BOTTLE in 1 CARTON (69842-513-34) / 237 mL in 1 BOTTLE
Marketing
Marketing Status
Brand
adult tussin 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": "d736f5ac-144d-4073-a714-87afd3a864e3", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1790650"], "spl_set_id": ["2f1dc8f8-79c5-4724-99aa-a55330ed9d5f"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["CVS Pharmacy"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (69842-513-26) / 118 mL in 1 BOTTLE", "package_ndc": "69842-513-26", "marketing_start_date": "20220712"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (69842-513-34) / 237 mL in 1 BOTTLE", "package_ndc": "69842-513-34", "marketing_start_date": "20220719"}], "brand_name": "adult tussin dm", "product_id": "69842-513_d736f5ac-144d-4073-a714-87afd3a864e3", "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": "69842-513", "generic_name": "dextromethorphan hydrobromide, guaifenesin", "labeler_name": "CVS Pharmacy", "product_type": "HUMAN OTC DRUG", "brand_name_base": "adult tussin dm", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "20 mg/20mL"}, {"name": "GUAIFENESIN", "strength": "200 mg/20mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20220712", "listing_expiration_date": "20261231"}