Package 50580-437-02

Brand: sudafed pe sinus congestion

Generic: phenylephrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50580-437-02
Digits Only 5058043702
Product NDC 50580-437
Product ID 50580-437_21ad7bba-a836-8d9d-e063-6294a90a371d
Description

2 BLISTER PACK in 1 CARTON (50580-437-02) / 18 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2019-06-17
Brand sudafed pe sinus congestion
Generic phenylephrine hydrochloride
Sample Package No

Linked Drug Pages (1)

Sudafed PE Sinus Congestion ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "21ad7bba-a836-8d9d-e063-6294a90a371d", "openfda": {"upc": ["0300450581365"], "unii": ["04JA59TNSJ"], "rxcui": ["1049182", "1052767"], "spl_set_id": ["2ca08917-1a75-4365-8520-c083e6a4225a"], "manufacturer_name": ["Kenvue Brands LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (50580-437-01)  / 18 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "50580-437-01", "marketing_start_date": "20190617"}, {"sample": false, "description": "2 BLISTER PACK in 1 CARTON (50580-437-02)  / 18 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "50580-437-02", "marketing_start_date": "20190617"}, {"sample": false, "description": "3 CARTON in 1 PACKAGE (50580-437-03)  / 2 BLISTER PACK in 1 CARTON / 18 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "50580-437-03", "marketing_start_date": "20190903"}], "brand_name": "Sudafed PE Sinus Congestion", "product_id": "50580-437_21ad7bba-a836-8d9d-e063-6294a90a371d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "50580-437", "generic_name": "Phenylephrine Hydrochloride", "labeler_name": "Kenvue Brands LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sudafed PE Sinus Congestion", "active_ingredients": [{"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190617", "listing_expiration_date": "20261231"}