Package 71679-309-00

Brand: guaifenesin

Generic: guaifenesin
NDC Package

Package Facts

Identity

Package NDC 71679-309-00
Digits Only 7167930900
Product NDC 71679-309
Description

38500 TABLET in 1 BOTTLE (71679-309-00)

Marketing

Marketing Status
Marketed Since 2024-03-07
Brand guaifenesin
Generic guaifenesin
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "45395c54-4eb3-fd26-e063-6294a90a9f93", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0371679309023"], "unii": ["495W7451VQ"], "rxcui": ["359601"], "spl_set_id": ["31755594-3e1c-b290-e063-6394a90aba61"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Health Pharma USA LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "38500 TABLET in 1 BOTTLE (71679-309-00)", "package_ndc": "71679-309-00", "marketing_start_date": "20240307"}, {"sample": false, "description": "200 TABLET in 1 BOTTLE (71679-309-02)", "package_ndc": "71679-309-02", "marketing_start_date": "20240207"}], "brand_name": "Guaifenesin", "product_id": "71679-309_45395c54-4eb3-fd26-e063-6294a90a9f93", "dosage_form": "TABLET", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "71679-309", "generic_name": "Guaifenesin", "labeler_name": "Health Pharma USA LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Guaifenesin", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "400 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240207", "listing_expiration_date": "20261231"}