Package 54738-980-01

Brand: mucus relief

Generic: guaifenesin 200 mg
NDC Package

Package Facts

Identity

Package NDC 54738-980-01
Digits Only 5473898001
Product NDC 54738-980
Product ID 54738-980_73570295-8ab7-1c19-e053-2991aa0a6b82
Description

100 TABLET in 1 BOTTLE (54738-980-01)

Marketing

Marketing Status
Marketed Since 2016-03-01
Brand mucus relief
Generic guaifenesin 200 mg
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": "73570295-8ab7-1c19-e053-2991aa0a6b82", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["495W7451VQ"], "rxcui": ["197741"], "spl_set_id": ["e20927a1-d402-48c1-ba00-0745ddd0a0e7"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Richmond Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (54738-980-01)", "package_ndc": "54738-980-01", "marketing_start_date": "20160301"}], "brand_name": "Mucus Relief", "product_id": "54738-980_73570295-8ab7-1c19-e053-2991aa0a6b82", "dosage_form": "TABLET", "product_ndc": "54738-980", "generic_name": "Guaifenesin 200 mg", "labeler_name": "Richmond Pharmaceuticals, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "200 mg/1"}], "application_number": "part341", "marketing_category": "OTC MONOGRAPH FINAL", "marketing_start_date": "20160301", "listing_expiration_date": "20261231"}