hydroxyzine hydrochloride
Generic: hydroxyzine hydrochloride
Labeler: chartwell rx, llcDrug Facts
Product Profile
Brand Name
hydroxyzine hydrochloride
Generic Name
hydroxyzine hydrochloride
Labeler
chartwell rx, llc
Dosage Form
SOLUTION
Routes
Active Ingredients
hydroxyzine dihydrochloride 10 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
62135-502
Product ID
62135-502_0770c6f3-a76a-819c-e063-6294a90a3cd8
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA201674
Listing Expiration
2026-12-31
Marketing Start
2013-08-21
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
62135502
Hyphenated Format
62135-502
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
hydroxyzine hydrochloride (source: ndc)
Generic Name
hydroxyzine hydrochloride (source: ndc)
Application Number
ANDA201674 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/5mL
Packaging
- 473 mL in 1 BOTTLE (62135-502-47)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0770c6f3-a76a-819c-e063-6294a90a3cd8", "openfda": {"upc": ["0362135502478"], "unii": ["76755771U3"], "rxcui": ["995241"], "spl_set_id": ["4590101d-7fb2-478b-acc5-bc9bdbb38ca9"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (62135-502-47)", "package_ndc": "62135-502-47", "marketing_start_date": "20221003"}], "brand_name": "Hydroxyzine Hydrochloride", "product_id": "62135-502_0770c6f3-a76a-819c-e063-6294a90a3cd8", "dosage_form": "SOLUTION", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "62135-502", "generic_name": "Hydroxyzine Hydrochloride", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxyzine Hydrochloride", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "10 mg/5mL"}], "application_number": "ANDA201674", "marketing_category": "ANDA", "marketing_start_date": "20130821", "listing_expiration_date": "20261231"}