hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride

Labeler: heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name hydroxyzine hydrochloride
Generic Name hydroxyzine hydrochloride
Labeler heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

hydroxyzine dihydrochloride 25 mg/1

Manufacturer
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 23155-501
Product ID 23155-501_2be52341-592e-4a89-acc0-730b0560b132
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 23155501
Hyphenated Format 23155-501

Supplemental Identifiers

RxCUI
995218 995258 995281
UPC
0323155500011 0323155502015 0323155501018
UNII
76755771U3

Packaging Origin

Original Packager
true

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
  • 100 TABLET in 1 BOTTLE (23155-501-01)
  • 500 TABLET in 1 BOTTLE (23155-501-05)
  • 1000 TABLET in 1 BOTTLE (23155-501-10)
source: ndc

Packages (3)

23155-501-01 100 TABLET in 1 BOTTLE (23155-501-01) 23155-501-05 500 TABLET in 1 BOTTLE (23155-501-05) 23155-501-10 1000 TABLET in 1 BOTTLE (23155-501-10)

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": "2be52341-592e-4a89-acc0-730b0560b132", "openfda": {"upc": ["0323155500011", "0323155502015", "0323155501018"], "unii": ["76755771U3"], "rxcui": ["995218", "995258", "995281"], "spl_set_id": ["f9ff4b7c-dc81-47af-8371-5c681eb0d876"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (23155-501-01)", "package_ndc": "23155-501-01", "marketing_start_date": "20140820"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (23155-501-05)", "package_ndc": "23155-501-05", "marketing_start_date": "20140820"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (23155-501-10)", "package_ndc": "23155-501-10", "marketing_start_date": "20140820"}], "brand_name": "Hydroxyzine hydrochloride", "product_id": "23155-501_2be52341-592e-4a89-acc0-730b0560b132", "dosage_form": "TABLET", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "23155-501", "generic_name": "Hydroxyzine hydrochloride", "labeler_name": "Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.", "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"}