cetirizine hydrochloride
Generic: cetirizine hydrochloride
Labeler: bionpharma inc.Drug Facts
Product Profile
Brand Name
cetirizine hydrochloride
Generic Name
cetirizine hydrochloride
Labeler
bionpharma inc.
Dosage Form
SOLUTION
Routes
Active Ingredients
cetirizine hydrochloride 1 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
69452-426
Product ID
69452-426_41d79fc7-75b2-120e-e063-6294a90a2f0c
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA078488
Listing Expiration
2026-12-31
Marketing Start
2025-12-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
69452426
Hyphenated Format
69452-426
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
cetirizine hydrochloride (source: ndc)
Generic Name
cetirizine hydrochloride (source: ndc)
Application Number
ANDA078488 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/mL
Packaging
- 120 mL in 1 BOTTLE (69452-426-55)
- 480 mL in 1 BOTTLE (69452-426-88)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "41d79fc7-75b2-120e-e063-6294a90a2f0c", "openfda": {"upc": ["0369452426555", "0369452426883"], "unii": ["64O047KTOA"], "rxcui": ["1014673"], "spl_set_id": ["41d7af88-87b4-370e-e063-6294a90a8af6"], "manufacturer_name": ["Bionpharma Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 mL in 1 BOTTLE (69452-426-55)", "package_ndc": "69452-426-55", "marketing_start_date": "20251201"}, {"sample": false, "description": "480 mL in 1 BOTTLE (69452-426-88)", "package_ndc": "69452-426-88", "marketing_start_date": "20251201"}], "brand_name": "Cetirizine Hydrochloride", "product_id": "69452-426_41d79fc7-75b2-120e-e063-6294a90a2f0c", "dosage_form": "SOLUTION", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "69452-426", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "Bionpharma Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cetirizine Hydrochloride", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "1 mg/mL"}], "application_number": "ANDA078488", "marketing_category": "ANDA", "marketing_start_date": "20251201", "listing_expiration_date": "20261231"}