Package 63868-753-50
Brand: quality choice mucus relief dm dm
Generic: dextromethorphan hydrobromide / guaifenesinPackage Facts
Identity
Package NDC
63868-753-50
Digits Only
6386875350
Product NDC
63868-753
Description
1 BOTTLE in 1 CARTON (63868-753-50) / 50 TABLET in 1 BOTTLE
Marketing
Marketing Status
Brand
quality choice mucus 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": "07b36c8b-1869-45d2-90be-b40b0fdb4f65", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0635515955721"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1147685"], "spl_set_id": ["1c33a01f-1186-4a19-b639-a9cd49245220"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Chain Drug Marketing Association"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (63868-753-50) / 50 TABLET in 1 BOTTLE", "package_ndc": "63868-753-50", "marketing_start_date": "20120801"}], "brand_name": "Quality Choice Mucus Relief DM DM", "product_id": "63868-753_07b36c8b-1869-45d2-90be-b40b0fdb4f65", "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": "63868-753", "generic_name": "Dextromethorphan Hydrobromide / Guaifenesin", "labeler_name": "Chain Drug Marketing Association", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Quality Choice Mucus 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"}