Package 41226-272-03

Brand: mucus relief

Generic: guaifenesin
NDC Package

Package Facts

Identity

Package NDC 41226-272-03
Digits Only 4122627203
Product NDC 41226-272
Description

30 TABLET in 1 BOTTLE (41226-272-03)

Marketing

Marketing Status
Marketed Since 2019-06-03
Brand mucus relief
Generic guaifenesin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "88f1545a-6dbd-54f8-e053-2995a90a4138", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["495W7451VQ"], "rxcui": ["359601"], "spl_set_id": ["813b1db2-a177-77c6-e053-2a91aa0ac73b"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["KROGER COMPANY"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (41226-272-03)", "package_ndc": "41226-272-03", "marketing_start_date": "20190603"}], "brand_name": "MUCUS RELIEF", "product_id": "41226-272_88f1545a-6dbd-54f8-e053-2995a90a4138", "dosage_form": "TABLET", "product_ndc": "41226-272", "generic_name": "Guaifenesin", "labeler_name": "KROGER COMPANY", "product_type": "HUMAN OTC DRUG", "brand_name_base": "MUCUS RELIEF", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "400 mg/1"}], "application_number": "part341", "marketing_category": "OTC MONOGRAPH FINAL", "marketing_start_date": "20190603", "listing_expiration_date": "20261231"}