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 50 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-2614
Product ID 50090-2614_18cd1ec0-5aa3-4bb3-8415-ef4d9079e190
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040840
Listing Expiration 2026-12-31
Marketing Start 2009-11-11

Pharmacologic Class

Classes
antihistamine [epc] histamine receptor antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500902614
Hyphenated Format 50090-2614

Supplemental Identifiers

RxCUI
995281
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 ANDA040840 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (50090-2614-0)
  • 30 TABLET in 1 BOTTLE (50090-2614-1)
  • 17 TABLET in 1 BOTTLE (50090-2614-3)
  • 25 TABLET in 1 BOTTLE (50090-2614-4)
source: ndc

Packages (4)

50090-2614-0 100 TABLET in 1 BOTTLE (50090-2614-0) 50090-2614-1 30 TABLET in 1 BOTTLE (50090-2614-1) 50090-2614-3 17 TABLET in 1 BOTTLE (50090-2614-3) 50090-2614-4 25 TABLET in 1 BOTTLE (50090-2614-4)

Ingredients (1)

hydroxyzine dihydrochloride (50 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": "18cd1ec0-5aa3-4bb3-8415-ef4d9079e190", "openfda": {"unii": ["76755771U3"], "rxcui": ["995281"], "spl_set_id": ["be6a2f09-c0f3-44e2-aac3-37e3702b93f0"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (50090-2614-0)", "package_ndc": "50090-2614-0", "marketing_start_date": "20181019"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-2614-1)", "package_ndc": "50090-2614-1", "marketing_start_date": "20161111"}, {"sample": false, "description": "17 TABLET in 1 BOTTLE (50090-2614-3)", "package_ndc": "50090-2614-3", "marketing_start_date": "20180807"}, {"sample": false, "description": "25 TABLET in 1 BOTTLE (50090-2614-4)", "package_ndc": "50090-2614-4", "marketing_start_date": "20180807"}], "brand_name": "HydrOXYzine Hydrochloride", "product_id": "50090-2614_18cd1ec0-5aa3-4bb3-8415-ef4d9079e190", "dosage_form": "TABLET", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "50090-2614", "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": "50 mg/1"}], "application_number": "ANDA040840", "marketing_category": "ANDA", "marketing_start_date": "20091111", "listing_expiration_date": "20261231"}