cetirizine hydrochloride
Generic: cetirizine hydrochloride
Labeler: preferred pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
cetirizine hydrochloride
Generic Name
cetirizine hydrochloride
Labeler
preferred pharmaceuticals inc.
Dosage Form
SOLUTION
Routes
Active Ingredients
cetirizine hydrochloride 1 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
68788-8523
Product ID
68788-8523_2b047f42-123a-4fc8-a8cf-fe2820788c12
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA078398
Listing Expiration
2026-12-31
Marketing Start
2023-09-13
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
687888523
Hyphenated Format
68788-8523
Supplemental Identifiers
RxCUI
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
ANDA078398 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/mL
Packaging
- 1 BOTTLE in 1 CARTON (68788-8523-1) / 120 mL in 1 BOTTLE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2b047f42-123a-4fc8-a8cf-fe2820788c12", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014673"], "spl_set_id": ["e874264a-becc-45d0-b934-779eab5f5085"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (68788-8523-1) / 120 mL in 1 BOTTLE", "package_ndc": "68788-8523-1", "marketing_start_date": "20230913"}], "brand_name": "Cetirizine Hydrochloride", "product_id": "68788-8523_2b047f42-123a-4fc8-a8cf-fe2820788c12", "dosage_form": "SOLUTION", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "68788-8523", "generic_name": "Cetirizine hydrochloride", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cetirizine Hydrochloride", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "1 mg/mL"}], "application_number": "ANDA078398", "marketing_category": "ANDA", "marketing_start_date": "20230913", "listing_expiration_date": "20261231"}