Package 80513-413-11

Brand: guaifenesin

Generic: guaifenesin
NDC Package

Package Facts

Identity

Package NDC 80513-413-11
Digits Only 8051341311
Product NDC 80513-413
Product ID 80513-413_41cfe010-f8b2-f181-e063-6394a90af095
Description

110 TABLET, EXTENDED RELEASE in 1 BOTTLE (80513-413-11)

Marketing

Marketing Status
Marketed Since 2025-07-01
Brand guaifenesin
Generic guaifenesin
Sample Package No

Linked Drug Pages (1)

GUAIFENESIN ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "41cfe010-f8b2-f181-e063-6394a90af095", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["495W7451VQ"], "rxcui": ["310621"], "spl_set_id": ["cb7cd1df-8cfb-4a9c-9567-809a2343622e"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Advanced Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "110 TABLET, EXTENDED RELEASE in 1 BOTTLE (80513-413-11)", "package_ndc": "80513-413-11", "marketing_start_date": "20250701"}], "brand_name": "GUAIFENESIN", "product_id": "80513-413_41cfe010-f8b2-f181-e063-6394a90af095", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "80513-413", "generic_name": "GUAIFENESIN", "labeler_name": "Advanced Rx LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "GUAIFENESIN", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "1200 mg/1"}], "application_number": "ANDA213420", "marketing_category": "ANDA", "marketing_start_date": "20201218", "listing_expiration_date": "20261231"}