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
Routes
ORAL
Active Ingredients

hydroxyzine dihydrochloride 25 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-2648
Product ID 50090-2648_2edc409b-5617-49f2-95d6-4487dc3a230c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204279
Listing Expiration 2026-12-31
Marketing Start 2014-08-20

Pharmacologic Class

Classes
antihistamine [epc] histamine receptor antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500902648
Hyphenated Format 50090-2648

Supplemental Identifiers

RxCUI
995218 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 ANDA204279 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 20 TABLET in 1 BOTTLE, PLASTIC (50090-2648-0)
  • 30 TABLET in 1 BOTTLE (50090-2648-1)
  • 60 TABLET in 1 BOTTLE (50090-2648-4)
  • 15 TABLET in 1 BOTTLE (50090-2648-6)
source: ndc

Packages (4)

50090-2648-0 20 TABLET in 1 BOTTLE, PLASTIC (50090-2648-0) 50090-2648-1 30 TABLET in 1 BOTTLE (50090-2648-1) 50090-2648-4 60 TABLET in 1 BOTTLE (50090-2648-4) 50090-2648-6 15 TABLET in 1 BOTTLE (50090-2648-6)

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": "2edc409b-5617-49f2-95d6-4487dc3a230c", "openfda": {"unii": ["76755771U3"], "rxcui": ["995218", "995258"], "spl_set_id": ["b52e1759-8be3-4e46-a891-4eaa9270c421"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE, PLASTIC (50090-2648-0)", "package_ndc": "50090-2648-0", "marketing_start_date": "20141128"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-2648-1)", "package_ndc": "50090-2648-1", "marketing_start_date": "20181112"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (50090-2648-4)", "package_ndc": "50090-2648-4", "marketing_start_date": "20161128"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE (50090-2648-6)", "package_ndc": "50090-2648-6", "marketing_start_date": "20181112"}], "brand_name": "Hydroxyzine hydrochloride", "product_id": "50090-2648_2edc409b-5617-49f2-95d6-4487dc3a230c", "dosage_form": "TABLET", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "50090-2648", "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": "ANDA204279", "marketing_category": "ANDA", "marketing_start_date": "20140820", "listing_expiration_date": "20261231"}