hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name hydroxyzine hydrochloride
Generic Name hydroxyzine hydrochloride
Labeler a-s medication solutions
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

hydroxyzine dihydrochloride 25 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7330
Product ID 50090-7330_4278def4-d310-40ba-a058-2b4f21b9d8ec
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA217652
Listing Expiration 2026-12-31
Marketing Start 2023-08-22

Pharmacologic Class

Classes
antihistamine [epc] histamine receptor antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500907330
Hyphenated Format 50090-7330

Supplemental Identifiers

RxCUI
995258
UNII
76755771U3

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 ANDA217652 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 20 TABLET, FILM COATED in 1 BOTTLE (50090-7330-0)
  • 30 TABLET, FILM COATED in 1 BOTTLE (50090-7330-1)
  • 60 TABLET, FILM COATED in 1 BOTTLE (50090-7330-4)
  • 15 TABLET, FILM COATED in 1 BOTTLE (50090-7330-6)
source: ndc

Packages (4)

50090-7330-0 20 TABLET, FILM COATED in 1 BOTTLE (50090-7330-0) 50090-7330-1 30 TABLET, FILM COATED in 1 BOTTLE (50090-7330-1) 50090-7330-4 60 TABLET, FILM COATED in 1 BOTTLE (50090-7330-4) 50090-7330-6 15 TABLET, FILM COATED in 1 BOTTLE (50090-7330-6)

Ingredients (1)

hydroxyzine dihydrochloride (25 mg/1)

Linked Drug Pages (1)

HYDROXYZINE HYDROCHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4278def4-d310-40ba-a058-2b4f21b9d8ec", "openfda": {"unii": ["76755771U3"], "rxcui": ["995258"], "spl_set_id": ["69a58bc6-c8a4-48ad-ac77-90fac42e0398"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (50090-7330-0)", "package_ndc": "50090-7330-0", "marketing_start_date": "20241015"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-7330-1)", "package_ndc": "50090-7330-1", "marketing_start_date": "20241015"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (50090-7330-4)", "package_ndc": "50090-7330-4", "marketing_start_date": "20241015"}, {"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE (50090-7330-6)", "package_ndc": "50090-7330-6", "marketing_start_date": "20241015"}], "brand_name": "HYDROXYZINE HYDROCHLORIDE", "product_id": "50090-7330_4278def4-d310-40ba-a058-2b4f21b9d8ec", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "50090-7330", "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": "ANDA217652", "marketing_category": "ANDA", "marketing_start_date": "20230822", "listing_expiration_date": "20261231"}