Package 0121-0744-04

Brand: guaifenesin

Generic: guaifenesin
NDC Package

Package Facts

Identity

Package NDC 0121-0744-04
Digits Only 0121074404
Product NDC 0121-0744
Description

118 mL in 1 BOTTLE (0121-0744-04)

Marketing

Marketing Status
Marketed Since 2002-09-01
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": "25a970c7-0016-4f22-9e94-1e20e1319e3e", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["495W7451VQ"], "rxcui": ["310604"], "spl_set_id": ["c2e53fb5-2798-47c8-9285-d1077d46e629"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["PAI Holdings, LLC dba PAI Pharma"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "118 mL in 1 BOTTLE (0121-0744-04)", "package_ndc": "0121-0744-04", "marketing_start_date": "20020901"}, {"sample": false, "description": "237 mL in 1 BOTTLE (0121-0744-08)", "package_ndc": "0121-0744-08", "marketing_start_date": "20020901"}, {"sample": false, "description": "473 mL in 1 BOTTLE (0121-0744-16)", "package_ndc": "0121-0744-16", "marketing_start_date": "20020901"}], "brand_name": "GUAIFENESIN", "product_id": "0121-0744_25a970c7-0016-4f22-9e94-1e20e1319e3e", "dosage_form": "SOLUTION", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "0121-0744", "generic_name": "GUAIFENESIN", "labeler_name": "PAI Holdings, LLC dba PAI Pharma", "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": "20020901", "listing_expiration_date": "20261231"}