Package 50580-436-01

Brand: sudafed pe head congestion plus pain

Generic: ibuprofen and phenylephrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50580-436-01
Digits Only 5058043601
Product NDC 50580-436
Description

2 BLISTER PACK in 1 CARTON (50580-436-01) / 10 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2019-06-17
Brand sudafed pe head congestion plus pain
Generic ibuprofen and phenylephrine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2ffbcc44-0ef3-b149-e063-6394a90ae7f5", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0300450551207"], "unii": ["WK2XYI10QM", "04JA59TNSJ"], "rxcui": ["1369775"], "spl_set_id": ["76513fb2-7323-4f1f-8a10-92f8f603cf97"], "pharm_class_cs": ["Anti-Inflammatory Agents, Non-Steroidal [CS]"], "pharm_class_epc": ["Nonsteroidal Anti-inflammatory Drug [EPC]"], "pharm_class_moa": ["Cyclooxygenase Inhibitors [MoA]"], "manufacturer_name": ["Kenvue Brands LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (50580-436-01)  / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "50580-436-01", "marketing_start_date": "20190617"}], "brand_name": "Sudafed PE Head Congestion Plus Pain", "product_id": "50580-436_2ffbcc44-0ef3-b149-e063-6394a90ae7f5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "50580-436", "generic_name": "Ibuprofen and Phenylephrine Hydrochloride", "labeler_name": "Kenvue Brands LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sudafed PE Head Congestion Plus Pain", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA203200", "marketing_category": "ANDA", "marketing_start_date": "20190617", "listing_expiration_date": "20261231"}