hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride

Labeler: preferred pharmaceuticals incl
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name hydroxyzine hydrochloride
Generic Name hydroxyzine hydrochloride
Labeler preferred pharmaceuticals incl
Dosage Form TABLET
Routes
ORAL
Active Ingredients

hydroxyzine dihydrochloride 25 mg/1

Manufacturer
Preferred Pharmaceuticals Incl

Identifiers & Regulatory

Product NDC 68788-7854
Product ID 68788-7854_d2ffcd08-7f0a-4113-aef3-050e49e7d4ee
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204279
Listing Expiration 2026-12-31
Marketing Start 2021-01-29

Pharmacologic Class

Classes
antihistamine [epc] histamine receptor antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687887854
Hyphenated Format 68788-7854

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 ANDA204279 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (68788-7854-3)
  • 60 TABLET in 1 BOTTLE (68788-7854-6)
  • 90 TABLET in 1 BOTTLE (68788-7854-9)
source: ndc

Packages (3)

68788-7854-3 30 TABLET in 1 BOTTLE (68788-7854-3) 68788-7854-6 60 TABLET in 1 BOTTLE (68788-7854-6) 68788-7854-9 90 TABLET in 1 BOTTLE (68788-7854-9)

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": "d2ffcd08-7f0a-4113-aef3-050e49e7d4ee", "openfda": {"unii": ["76755771U3"], "rxcui": ["995258"], "spl_set_id": ["63fdf791-1a58-45ba-8ef2-15b80bb24f23"], "manufacturer_name": ["Preferred Pharmaceuticals Incl"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-7854-3)", "package_ndc": "68788-7854-3", "marketing_start_date": "20210129"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68788-7854-6)", "package_ndc": "68788-7854-6", "marketing_start_date": "20210129"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-7854-9)", "package_ndc": "68788-7854-9", "marketing_start_date": "20210129"}], "brand_name": "Hydroxyzine hydrochloride", "product_id": "68788-7854_d2ffcd08-7f0a-4113-aef3-050e49e7d4ee", "dosage_form": "TABLET", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "68788-7854", "generic_name": "Hydroxyzine hydrochloride", "labeler_name": "Preferred Pharmaceuticals Incl", "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": "20210129", "listing_expiration_date": "20261231"}