Package 72090-009-01

Brand: mucus relief

Generic: guaifenesin 400 mg
NDC Package

Package Facts

Identity

Package NDC 72090-009-01
Digits Only 7209000901
Product NDC 72090-009
Product ID 72090-009_9f130a45-ac52-42e1-aff0-60eeb6492505
Description

200 TABLET in 1 BOTTLE (72090-009-01)

Marketing

Marketing Status
Marketed Since 2024-01-19
Brand mucus relief
Generic guaifenesin 400 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": "9f130a45-ac52-42e1-aff0-60eeb6492505", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["495W7451VQ"], "rxcui": ["359601"], "spl_set_id": ["3b7e0ee7-4dda-4bbe-842c-6cbbc208acd5"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Pioneer Life Sciences, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 TABLET in 1 BOTTLE (72090-009-01)", "package_ndc": "72090-009-01", "marketing_start_date": "20240119"}], "brand_name": "MUCUS RELIEF", "product_id": "72090-009_9f130a45-ac52-42e1-aff0-60eeb6492505", "dosage_form": "TABLET", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "72090-009", "generic_name": "guaifenesin 400 mg", "labeler_name": "Pioneer Life Sciences, LLC", "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_start_date": "20240119", "listing_expiration_date": "20261231"}