hydroxyzine hydrochloride
Generic: hydroxyzine hydrochloride
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
hydroxyzine hydrochloride
Generic Name
hydroxyzine hydrochloride
Labeler
a-s medication solutions
Dosage Form
TABLET
Routes
Active Ingredients
hydroxyzine dihydrochloride 25 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-7582
Product ID
50090-7582_d0abf9e3-d92e-445f-b626-a81b499d6e47
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA040840
Listing Expiration
2026-12-31
Marketing Start
2009-11-11
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500907582
Hyphenated Format
50090-7582
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
hydroxyzine hydrochloride (source: ndc)
Generic Name
hydroxyzine hydrochloride (source: ndc)
Application Number
ANDA040840 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 mg/1
Packaging
- 28 TABLET in 1 BOTTLE (50090-7582-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d0abf9e3-d92e-445f-b626-a81b499d6e47", "openfda": {"unii": ["76755771U3"], "rxcui": ["995258"], "spl_set_id": ["723b810b-46cc-4c45-ae1f-93ca358e007d"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "28 TABLET in 1 BOTTLE (50090-7582-1)", "package_ndc": "50090-7582-1", "marketing_start_date": "20250618"}], "brand_name": "HydrOXYzine Hydrochloride", "product_id": "50090-7582_d0abf9e3-d92e-445f-b626-a81b499d6e47", "dosage_form": "TABLET", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "50090-7582", "generic_name": "HydrOXYzine Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HydrOXYzine Hydrochloride", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA040840", "marketing_category": "ANDA", "marketing_start_date": "20091111", "listing_expiration_date": "20261231"}