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
63629-2533
Product ID
63629-2533_acc7fd37-12cc-4319-ac53-eb35e3e18d04
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
636292533
Hyphenated Format
63629-2533
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
- 1 BOTTLE in 1 CARTON (63629-2533-1) / 148 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": "acc7fd37-12cc-4319-ac53-eb35e3e18d04", "openfda": {"unii": ["SOD6A38AGA"], "rxcui": ["855168"], "spl_set_id": ["628c26f0-f6bb-4658-ba50-8ca04cd859cb"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (63629-2533-1) / 148 mL in 1 BOTTLE", "package_ndc": "63629-2533-1", "marketing_start_date": "20111107"}], "brand_name": "levocetirizine dihydrochloride", "product_id": "63629-2533_acc7fd37-12cc-4319-ac53-eb35e3e18d04", "dosage_form": "SOLUTION", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "63629-2533", "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"}