Package 0363-6150-09

Brand: severe sinus congestion

Generic: acetaminophen, guaifenesin, phenylephrine hcl
NDC Package

Package Facts

Identity

Package NDC 0363-6150-09
Digits Only 0363615009
Product NDC 0363-6150
Product ID 0363-6150_cd58f535-cc6e-41ef-8b2f-9c94eba189d2
Description

2 BLISTER PACK in 1 CARTON (0363-6150-09) / 10 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2013-06-30
Brand severe sinus congestion
Generic acetaminophen, guaifenesin, phenylephrine hcl
Sample Package No

Linked Drug Pages (1)

Severe Sinus Congestion ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "cd58f535-cc6e-41ef-8b2f-9c94eba189d2", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0311917160399"], "unii": ["362O9ITL9D", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1243679"], "spl_set_id": ["8745d9d8-640d-4e3b-96fe-d25032c1e3ce"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Walgreen Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (0363-6150-09)  / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0363-6150-09", "marketing_start_date": "20130630"}], "brand_name": "Severe Sinus Congestion", "product_id": "0363-6150_cd58f535-cc6e-41ef-8b2f-9c94eba189d2", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "0363-6150", "generic_name": "Acetaminophen, Guaifenesin, Phenylephrine HCl", "labeler_name": "Walgreen Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Severe Sinus Congestion", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "GUAIFENESIN", "strength": "200 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20130630", "listing_expiration_date": "20261231"}