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
SYRUP
Routes
Active Ingredients
hydroxyzine dihydrochloride 10 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
62135-750
Product ID
62135-750_25117412-3663-105d-e063-6394a90a0d64
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA087294
Listing Expiration
2026-12-31
Marketing Start
1982-04-12
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
62135750
Hyphenated Format
62135-750
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
ANDA087294 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/5mL
Packaging
- 473 mL in 1 BOTTLE (62135-750-47)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "25117412-3663-105d-e063-6394a90a0d64", "openfda": {"upc": ["0362135750473"], "unii": ["76755771U3"], "rxcui": ["995241"], "spl_set_id": ["53b2d731-f38a-47c0-9e5c-abd3b45e2fe1"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (62135-750-47)", "package_ndc": "62135-750-47", "marketing_start_date": "20230809"}], "brand_name": "HYDROXYZINE HYDROCHLORIDE", "product_id": "62135-750_25117412-3663-105d-e063-6394a90a0d64", "dosage_form": "SYRUP", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "62135-750", "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": "ANDA087294", "marketing_category": "ANDA", "marketing_start_date": "19820412", "listing_expiration_date": "20261231"}