levocetirizine dihydrochloride
Generic: levocetirizine dihydrochloride
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
levocetirizine dihydrochloride
Generic Name
levocetirizine dihydrochloride
Labeler
bryant ranch prepack
Dosage Form
SOLUTION
Routes
Active Ingredients
levocetirizine dihydrochloride .5 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
72162-1424
Product ID
72162-1424_38cb0ddb-5227-4066-9b07-a1feececf7a3
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA091263
Listing Expiration
2026-12-31
Marketing Start
2011-11-07
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
721621424
Hyphenated Format
72162-1424
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
levocetirizine dihydrochloride (source: ndc)
Generic Name
levocetirizine dihydrochloride (source: ndc)
Application Number
ANDA091263 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .5 mg/mL
Packaging
- 148 mL in 1 BOTTLE (72162-1424-2)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "38cb0ddb-5227-4066-9b07-a1feececf7a3", "openfda": {"unii": ["SOD6A38AGA"], "rxcui": ["855168"], "spl_set_id": ["a9e7152c-0aa3-4355-8805-307e510ac86b"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "148 mL in 1 BOTTLE (72162-1424-2)", "package_ndc": "72162-1424-2", "marketing_start_date": "20230926"}], "brand_name": "levocetirizine dihydrochloride", "product_id": "72162-1424_38cb0ddb-5227-4066-9b07-a1feececf7a3", "dosage_form": "SOLUTION", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "72162-1424", "generic_name": "Levocetirizine dihydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "levocetirizine dihydrochloride", "active_ingredients": [{"name": "LEVOCETIRIZINE DIHYDROCHLORIDE", "strength": ".5 mg/mL"}], "application_number": "ANDA091263", "marketing_category": "ANDA", "marketing_start_date": "20111107", "listing_expiration_date": "20261231"}