Package 79481-5072-8

Brand: pressure, pain and mucus

Generic: acetaminophen, guaifenesin, phenylephrine hcl
NDC Package

Package Facts

Identity

Package NDC 79481-5072-8
Digits Only 7948150728
Product NDC 79481-5072
Description

2 BLISTER PACK in 1 CARTON (79481-5072-8) / 12 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2024-07-16
Brand pressure, pain and mucus
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": "07497ab8-6b58-491e-83af-304795a3e936", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0713733971942"], "unii": ["362O9ITL9D", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1243679"], "spl_set_id": ["7d42e164-86e9-4baa-a389-3271cf99920e"], "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 (79481-5072-8)  / 12 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "79481-5072-8", "marketing_start_date": "20240716"}], "brand_name": "Pressure, Pain and Mucus", "product_id": "79481-5072_07497ab8-6b58-491e-83af-304795a3e936", "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": "79481-5072", "generic_name": "Acetaminophen, Guaifenesin, Phenylephrine HCl", "labeler_name": "Meijer Distribution, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pressure, Pain and Mucus", "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": "20240716", "listing_expiration_date": "20261231"}