Package 50580-447-01
Brand: sudafed pe head congestion plus mucus
Generic: acetaminophen, guaifenesin, and phenylephrine hydrochloridePackage Facts
Identity
Package NDC
50580-447-01
Digits Only
5058044701
Product NDC
50580-447
Description
2 BLISTER PACK in 1 CARTON (50580-447-01) / 12 TABLET, FILM COATED in 1 BLISTER PACK
Marketing
Marketing Status
Brand
sudafed pe head congestion plus mucus
Generic
acetaminophen, guaifenesin, and phenylephrine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "21bd70b6-1f2f-75bc-e063-6294a90a61f3", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["362O9ITL9D", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1243679"], "spl_set_id": ["f0739186-41b9-4761-adf7-08101b30a18e"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Kenvue Brands LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (50580-447-01) / 12 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "50580-447-01", "marketing_start_date": "20190617"}], "brand_name": "SUDAFED PE Head Congestion Plus Mucus", "product_id": "50580-447_21bd70b6-1f2f-75bc-e063-6294a90a61f3", "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": "50580-447", "generic_name": "acetaminophen, guaifenesin, and phenylephrine hydrochloride", "labeler_name": "Kenvue Brands LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "SUDAFED PE Head Congestion Plus 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": "20190617", "listing_expiration_date": "20261231"}