Package 55681-301-01

Brand: mucus relief guaifenesin extended-release 600 mg

Generic: guaifenesin
NDC Package

Package Facts

Identity

Package NDC 55681-301-01
Digits Only 5568130101
Product NDC 55681-301
Description

100 TABLET in 1 BOTTLE (55681-301-01)

Marketing

Marketing Status
Marketed Since 2022-03-02
Brand mucus relief guaifenesin extended-release 600 mg
Generic guaifenesin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0e12d44c-f957-c1b1-e063-6394a90a7483", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["495W7451VQ"], "rxcui": ["636522"], "spl_set_id": ["d9d13c67-51a1-aa79-e053-2995a90abdbb"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["TWIN MED LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (55681-301-01)", "package_ndc": "55681-301-01", "marketing_start_date": "20220302"}], "brand_name": "MUCUS RELIEF GUAIFENESIN EXTENDED-RELEASE 600 mg", "product_id": "55681-301_0e12d44c-f957-c1b1-e063-6394a90a7483", "dosage_form": "TABLET", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "55681-301", "generic_name": "GUAIFENESIN", "labeler_name": "TWIN MED LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "MUCUS RELIEF", "brand_name_suffix": "GUAIFENESIN EXTENDED-RELEASE 600 mg", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "600 mg/1"}], "application_number": "ANDA213420", "marketing_category": "ANDA", "marketing_start_date": "20220302", "listing_expiration_date": "20261231"}