Package 79481-7250-8

Brand: sinus severe non drowsy, daytime

Generic: acetaminophen, guaifenesin, phenylephrine hcl
NDC Package

Package Facts

Identity

Package NDC 79481-7250-8
Digits Only 7948172508
Product NDC 79481-7250
Description

2 BLISTER PACK in 1 CARTON (79481-7250-8) / 12 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2024-06-11
Brand sinus severe non drowsy, daytime
Generic acetaminophen, guaifenesin, phenylephrine hcl
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6406edfe-8b49-4356-a556-2433d1aebd9f", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0713733971928"], "unii": ["362O9ITL9D", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1243679"], "spl_set_id": ["84c30ec9-a7b5-4d2f-95b2-d6fb895945de"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Meijer Distribution, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (79481-7250-8)  / 12 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "79481-7250-8", "marketing_start_date": "20240611"}], "brand_name": "Sinus Severe Non Drowsy, Daytime", "product_id": "79481-7250_6406edfe-8b49-4356-a556-2433d1aebd9f", "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": "79481-7250", "generic_name": "Acetaminophen, Guaifenesin, Phenylephrine HCl", "labeler_name": "Meijer Distribution, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sinus Severe", "brand_name_suffix": "Non Drowsy, Daytime", "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": "20240611", "listing_expiration_date": "20261231"}