cetirizine hydrochloride
Generic: cetirizine hydrochloride
Labeler: cardinal health 107, llcDrug Facts
Product Profile
Brand Name
cetirizine hydrochloride
Generic Name
cetirizine hydrochloride
Labeler
cardinal health 107, llc
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
cetirizine hydrochloride 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
55154-5399
Product ID
55154-5399_897f5838-b1e4-472f-9348-f001dd1d5f22
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA076677
Listing Expiration
2026-12-31
Marketing Start
2012-03-30
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
551545399
Hyphenated Format
55154-5399
Supplemental Identifiers
RxCUI
UPC
UNII
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
cetirizine hydrochloride (source: ndc)
Generic Name
cetirizine hydrochloride (source: ndc)
Application Number
ANDA076677 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 10 BLISTER PACK in 1 BAG (55154-5399-0) / 1 TABLET, FILM COATED 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": "897f5838-b1e4-472f-9348-f001dd1d5f22", "openfda": {"upc": ["0055154539906"], "unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["0b0190c7-acfd-4140-bcaf-9fe835ebaf49"], "manufacturer_name": ["Cardinal Health 107, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 BAG (55154-5399-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "55154-5399-0", "marketing_start_date": "20120330"}], "brand_name": "Cetirizine Hydrochloride", "product_id": "55154-5399_897f5838-b1e4-472f-9348-f001dd1d5f22", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "55154-5399", "generic_name": "cetirizine hydrochloride", "labeler_name": "Cardinal Health 107, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cetirizine Hydrochloride", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA076677", "marketing_category": "ANDA", "marketing_start_date": "20120330", "listing_expiration_date": "20261231"}