Package 50580-363-02

Brand: sudafed sinus congestion

Generic: pseudoephedrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50580-363-02
Digits Only 5058036302
Product NDC 50580-363
Product ID 50580-363_21707bfd-d78e-0f04-e063-6294a90a8945
Description

2 BLISTER PACK in 1 CARTON (50580-363-02) / 12 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2021-07-31
Brand sudafed sinus congestion
Generic pseudoephedrine hydrochloride
Sample Package No

Linked Drug Pages (1)

SUDAFED Sinus Congestion ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "21707bfd-d78e-0f04-e063-6294a90a8945", "openfda": {"upc": ["0300810865241"], "unii": ["6V9V2RYJ8N"], "rxcui": ["1049160", "1049529"], "spl_set_id": ["c05d7e27-6821-468f-b27d-9c0b02a07b0f"], "manufacturer_name": ["Kenvue Brands LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 BLISTER PACK in 1 CARTON (50580-363-01)  / 12 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "50580-363-01", "marketing_start_date": "20210731"}, {"sample": false, "description": "2 BLISTER PACK in 1 CARTON (50580-363-02)  / 12 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "50580-363-02", "marketing_start_date": "20210731"}, {"sample": false, "description": "3 CARTON in 1 PACKAGE (50580-363-03)  / 2 BLISTER PACK in 1 CARTON / 12 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "50580-363-03", "marketing_start_date": "20220207"}], "brand_name": "SUDAFED Sinus Congestion", "product_id": "50580-363_21707bfd-d78e-0f04-e063-6294a90a8945", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "50580-363", "generic_name": "Pseudoephedrine Hydrochloride", "labeler_name": "Kenvue Brands LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "SUDAFED Sinus Congestion", "active_ingredients": [{"name": "PSEUDOEPHEDRINE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210731", "listing_expiration_date": "20261231"}