zyrtec
Generic: cetirizine hydrochloride
Labeler: kenvue brands llcDrug Facts
Product Profile
Brand Name
zyrtec
Generic Name
cetirizine hydrochloride
Labeler
kenvue brands llc
Dosage Form
TABLET, CHEWABLE
Routes
Active Ingredients
cetirizine hydrochloride 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50580-753
Product ID
50580-753_375f333a-6e53-5140-e063-6294a90a9967
Product Type
HUMAN OTC DRUG
Marketing Category
NDA
Application Number
NDA021621
Listing Expiration
2026-12-31
Marketing Start
2022-06-20
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
50580753
Hyphenated Format
50580-753
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
zyrtec (source: ndc)
Generic Name
cetirizine hydrochloride (source: ndc)
Application Number
NDA021621 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 4 BLISTER PACK in 1 CARTON (50580-753-24) / 6 TABLET, CHEWABLE in 1 BLISTER PACK
Packages (1)
Ingredients (1)
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"}