Package 69729-788-20

Brand: tesalon tesaperlas severe cold max relief

Generic: dextromethorphan hbr, guaifenesin
NDC Package

Package 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
Marketed Since 2024-09-27
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"}