Package 81033-102-16

Brand: guaifenesin

Generic: guaifenesin
NDC Package

Package Facts

Identity

Package NDC 81033-102-16
Digits Only 8103310216
Product NDC 81033-102
Description

473 mL in 1 BOTTLE (81033-102-16)

Marketing

Marketing Status
Marketed Since 2025-04-01
Brand guaifenesin
Generic guaifenesin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "31b88302-3352-a500-e063-6294a90acce8", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["495W7451VQ"], "rxcui": ["310604"], "spl_set_id": ["31b8ad0a-3637-03db-e063-6394a90acdc3"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["KESIN PHARMA CORPORATION"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (81033-102-16)", "package_ndc": "81033-102-16", "marketing_start_date": "20250401"}], "brand_name": "Guaifenesin", "product_id": "81033-102_31b88302-3352-a500-e063-6294a90acce8", "dosage_form": "LIQUID", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "81033-102", "generic_name": "Guaifenesin", "labeler_name": "KESIN PHARMA CORPORATION", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Guaifenesin", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "100 mg/5mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250401", "listing_expiration_date": "20261231"}