Package 50580-116-30

Brand: zyrtec hives

Generic: cetirizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50580-116-30
Digits Only 5058011630
Product NDC 50580-116
Description

1 BOTTLE in 1 CARTON (50580-116-30) / 30 TABLET, FILM COATED in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2025-06-02
Brand zyrtec hives
Generic cetirizine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "37b38291-50c9-00c9-e063-6394a90a83ef", "openfda": {"upc": ["0300450138323"], "unii": ["64O047KTOA"], "rxcui": ["1014678", "1020026"], "spl_set_id": ["31136e3a-94fa-0860-e063-6394a90a008d"], "manufacturer_name": ["Kenvue Brands LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (50580-116-30)  / 30 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "50580-116-30", "marketing_start_date": "20250602"}], "brand_name": "ZYRTEC Hives", "product_id": "50580-116_37b38291-50c9-00c9-e063-6394a90a83ef", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "50580-116", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "Kenvue Brands LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ZYRTEC Hives", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "NDA019835", "marketing_category": "NDA", "marketing_start_date": "20250602", "listing_expiration_date": "20261231"}