Package 50580-753-24

Brand: zyrtec

Generic: cetirizine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50580-753-24
Digits Only 5058075324
Product NDC 50580-753
Description

4 BLISTER PACK in 1 CARTON (50580-753-24) / 6 TABLET, CHEWABLE in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2022-06-20
Brand zyrtec
Generic cetirizine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "375f333a-6e53-5140-e063-6294a90a9967", "openfda": {"upc": ["0300450250247"], "unii": ["64O047KTOA"], "rxcui": ["1014674", "1020022"], "spl_set_id": ["dc613bd5-70fd-1d9b-e053-2995a90a41cd"], "manufacturer_name": ["Kenvue Brands LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 BLISTER PACK in 1 CARTON (50580-753-24)  / 6 TABLET, CHEWABLE in 1 BLISTER PACK", "package_ndc": "50580-753-24", "marketing_start_date": "20220620"}], "brand_name": "Zyrtec", "product_id": "50580-753_375f333a-6e53-5140-e063-6294a90a9967", "dosage_form": "TABLET, CHEWABLE", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "50580-753", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "Kenvue Brands LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Zyrtec", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "NDA021621", "marketing_category": "NDA", "marketing_start_date": "20220620", "listing_expiration_date": "20261231"}