Package 69729-788-20
Brand: tesalon tesaperlas severe cold max relief
Generic: dextromethorphan hbr, guaifenesinPackage Facts
Identity
Package NDC
69729-788-20
Digits Only
6972978820
Product NDC
69729-788
Description
1 BLISTER PACK in 1 CARTON (69729-788-20) / 20 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Marketing
Marketing Status
Brand
tesalon tesaperlas severe cold max relief
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": "4769d8b1-87ce-a188-e063-6294a90aa026", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0850043169123"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1661740"], "spl_set_id": ["23223821-4fa0-5d99-e063-6394a90af0e5"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["OPMX LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (69729-788-20) / 20 CAPSULE, LIQUID FILLED in 1 BLISTER PACK", "package_ndc": "69729-788-20", "marketing_start_date": "20240927"}], "brand_name": "TESALON Tesaperlas Severe Cold Max Relief", "product_id": "69729-788_4769d8b1-87ce-a188-e063-6294a90aa026", "dosage_form": "CAPSULE, LIQUID FILLED", "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": "69729-788", "generic_name": "Dextromethorphan HBr, Guaifenesin", "labeler_name": "OPMX LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "TESALON Tesaperlas Severe Cold Max Relief", "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": "20240927", "listing_expiration_date": "20271231"}