Package 68016-545-50

Brand: Mucus Relief

Generic: Guaifenesin
NDC Package

Package Facts

Identity

Package NDC 68016-545-50
Digits Only 6801654550
Product NDC 68016-545
Product ID 68016-545_3bb70627-72dc-4e52-95a4-d23661a5ffb5
Description

1 BOTTLE, PLASTIC in 1 CARTON (68016-545-50) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Discontinued 2026-02-28
Brand Mucus Relief
Generic Guaifenesin
Sample Package No

Linked Drug Pages (1)

Mucus Relief ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3bb70627-72dc-4e52-95a4-d23661a5ffb5", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0840986037696"], "unii": ["495W7451VQ"], "rxcui": ["359601"], "spl_set_id": ["b2e88323-5af9-4ec8-bb98-4da0a774e54e"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Chain Drug Consortium"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (68016-545-50)  / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "68016-545-50", "marketing_end_date": "20260228", "marketing_start_date": "20230109"}], "brand_name": "Mucus Relief", "product_id": "68016-545_3bb70627-72dc-4e52-95a4-d23661a5ffb5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "68016-545", "generic_name": "Guaifenesin", "labeler_name": "Chain Drug Consortium", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "400 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20260228", "marketing_start_date": "20230109"}