Package 41226-724-89

{"route": ["ORAL"], "spl_id": "194317de-d799-b556-e063-6394a90acff7", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["495W7451VQ"], "rxcui": ["310621"], "spl_set_id": ["100ff8e2-88ed-0e8c-e063-6294a90a5716"], "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": "1 BLISTER PACK in 1 CARTON (41226-724-89)  / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "41226-724-89", "marketing_start_date": "20240527"}], "brand_name": "Maximum Strength Mucus Relief", "product_id": "41226-724_194317de-d799-b556-e063-6394a90acff7", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "41226-724", "generic_name": "Guaifenesin", "labeler_name": "KROGER COMPANY", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Maximum Strength Mucus Relief", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "1200 mg/1"}], "application_number": "ANDA217780", "marketing_category": "ANDA", "marketing_start_date": "20240527", "listing_expiration_date": "20261231"}